Monthly Archives: March 2017

Is Clinical Research A Good Career Choice?

Clinical research is an exciting branch of medicine that determines the efficacy and safety of novel drugs. As a CRA one has a responsibility to make sure that data is gathered and handled according to strict guidelines. A CRA is a link between medical doctors, trial patients and pharma companies or their representatives. There’s a great need for talented and skilled people in the business.

Is Clinical Research A Good Career Choice?

The biotechnology boom is creating more opportunities for clinical research professionals trained to aide bring the latest drug therapies from the laboratory to market. 

With plenty of job opportunities in the clinical research field today and for the coming future there is a huge demand to grow the drug pipelines swell.

Aside from the doctors, who investigate the effects of drug therapies on patiens, trials need clinical research coordinators (CRCs) and clinical research associates (CRAs) to make sure that testing is conducted according to strict FDA guidelines.

To make an entry into this field, a person must hold a degree of B.Sc. The clinical research sector could be joined after graduation in pharmacy, life science and medicine. Bioscience further includes sub-disciplines like genetics, botany, biochemistry and zoology. People with educational qualifications from these fields can try into this industry. Those aspirants who have a work experience of two or three years are given more preference.


The field has several branches. The common entry-level roles include the position of a
Clinical Research Associate (CRA). A CRA is a key person in the planning, execution and supervision of the trials. They also assist in the making of manuscripts and presentations from scientific meetings and technical journals and visit meetings and training programs. Hence there is a high demand for clinical research associate jobs for freshers. Clinical research also includes biostatistics. Biostatisticians do statistical works, programming, evaluation and summary-writing for clinical trial projects.

Another good post in this industry is of Clinical Research Managers (CRM). They manage the planning and writing of protocols, informed consent forms and case report forms for trials. They make sure the case report forms are regularly reviewed and handed over to the data management group. Similar positions are Clinical Research Coordinator, Clinical Research Investigator, Business Development Manager and Clinical Data Manager.

With the presence of multi-national companies who establish their research facilities in India and with upcoming clinical research organisations, clinical sector is likely to develop exponentially.

There are several institutes that offer clinical research programs. Among the top institutes of clinical research in Pune the name of CRB Tech Solutions is well heard. CRB Tech has created a niche for itself among courses in clinical research offering clinical research training institutes in Pune.

The Clinical Research Training program by CRB Tech Solutions provides all the guidance to key skills and knowledge in clinical research using an innovative method. The clinical research program is a 4 month certificate program consisting of lectures, live projects, internships and development of soft skills. The training program includes a detailed CRA course for your advantage.

The modules of Clinical Research Training Program are upgraded and redesigned on a periodical basis by our industry expert. There are regular campuses drives take. CRB Tech also provides training in aptitude which is a part of the syllabus as it enables one to successfully overcome the hardest of the aptitude tests, which one faces in the interviews

Participants who achieve all the program objectives, have cleared all their dues and have 90% attendance are granted a Certificate of Completion.

In the competition of many organizations CRB Tech Solutions developed a good name. It has earned a name in providing the best training in Clinical Research.

Clinical training jobs in Pune are increasing and to fulfill the current demand of the proficient candidates, you should consider enhancing yourself with our clinical research training program.

The Clinical Research review by CRB Tech Solutions will guide you in considering a clinical research career in this field 

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Clinical Research Training Program By CRB Tech Solutions

The Clinical Research Training program by CRB Tech Solutions   provides an introduction to key skills and knowledge in clinical research using an innovative method. The clinical research program is a four-month certificate program consisting of lectures, live projects, internships and development of soft skills. The program’s well blended curriculum emphasizes skill-based and team-based peer-to-peer learning. This program provides students in life sciences advanced training in the methods and conduct of clinical research.

Among the very few training institutes in Pune that offer clinical research courses, CRB Tech Solutions Pune offers real time and focused clinical research training program. Our program is designed to transform Life Sciences graduates into efficient professionals who will add value to the companies who hire them.

You might find other institutes of clinical research that provide clinical research training in Pune but the need to take the right decision and follow the right institute in making a bright career.

Objectives

After completing this program, you can be able to perform the following:

1. Observational and experimental clinical research.
2. Plan and implement a clinical trial.
3. Analyze and interpret clinical research data.

Candidates for This Program

Any one of the following minimum qualifications is eligible:

MBBS, BDS, BAMS, BHMS, B.PHARM, B.Sc. (Life sciences, Biotech, Nursing), Post Graduate Diploma

Why CRB Tech Solutions?

100 % placement guarantee on paper

We offer LOI (conditional offer letter) from our clients

Placement with lifetime support for alumni and fresher

Best in campus drives

Our mentors are corporate expertise faculties.

Training in German language

Personality development training to help you in developing soft skills that will set you ahead of your contemporaries.

95% practically oriented training sessions.

A Customised Training Program:

Detailed and expertise training is additionally offered alongside customized technical training to guarantee the general development of the students.

Foremost curriculum: The modules of Clinical Research Training Program are upgraded and redesigned on a periodical basis by our industry expert.

Regular campus drives take

Training in aptitude is a part of the syllabus as it enables you to successfully overcome the hardest of the aptitude tests, which you would face in the interviews.

Rules and Regulations:

Compulsory 90% classroom attendance.

Earn a support amount with no burden of fees.

Payment options:

Payment options for fees is flexible with the usage of either credit card or debit card.

Curriculum

The program curriculum consists of three modules which are again well divided to fit the period of training and for your ease. Throughout the program, trainees are expected to perform well and do and submit their task in time.

Module 1

Preclinical Research

  • Drug Discovery & Development
  • Preformulation Studies
  • Formulation & Ingredients
  • Animal Research And Trials
  • Introduction to Clinical research
  • Introduction to pharmaceuticals
  • History of Clinical Research

Module 2

Clinical Research (core)

Clinical research process flow

  • Guidelines for Good clinical practice (GCP)
  • Essential documents
  • Preparation of IB
  • Preparation of Protocol,CRF,ICF
  • Quality Analysis in Clinical Research

Bioethics and Clinical Research

  • How the ethics committee regulate
  • Pharmacovigilance
  • Regulatory affairs and regulatory submissions
  • Guidelines in clinical research
  • Career pathway in Clinical Research

Module 3

Clinical Data Management

  • Overview of Clinical Data Management
  • Overview of Electronic data Capture
  • Protocol Review
  • Data Management Plan
  • CRF Designing
  • Lab Data Handling
  • Database Designing and User Acceptance Testing
  • Medical Coding

I MedDRA

CD-9

  • Data Management Standards in Clinical Research – CDISC
  • Overview to Electronic Data Capture
  • Designing CRF in MS Word
  • Identifying disparities on CRF pages
  • How to generate queries for the sites

Course for General Aptitude

  • Percentages Profit And Loss
  • Number System
  • Simple Interest Compound Interest
  • Permutation And Combination
  • Probability
  • Number Series
  • Coding Decoding
  • Blood Relation
  • Puzzle-Based Problems

Participants who achieve all of the program objectives, have cleared all their dues and have 90% attendance are granted a Certificate of Completion.

The management reserves the rights to amend or modify its rules & regulations and schedules if a need arises and this will be applied to all the currently enrolled candidates in the ongoing program of Clinical Research Training.

CRB Tech Solutions can update the programs by making changes in title, contents, and structure.

The Clinical Research review by CRB Tech Solutions will guide you in considering a clinical research career in this field.

Related Post: 

  1. Clinical Research Courses,Training In Pune With 100% Job Guarantee
  2. Clinical Research Associate Training | Jobs In Pune

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Clinical Research Courses,Training In Pune With 100% Job Guarantee

India is becoming a Research hub and Clinical trial industry is pegging pegged over Rs 3,500 Crores and is growing at 10-12% annually. The clinical research sector is growing at an amazing rate and opening up a wide scope of career opportunities for trained professionals. There is a massive demand for Clinical Research professionals in clinical trial management, Clinical data Management and authorities regulating ethical issues related to clinical research. This makes it an interesting career option with massive growth potential.

Clinical Research Courses,Training In Pune With 100% Job Guarantee

Clinical research Industry is all set to become the next big thing in India. A large population with a good workforce and cost benefits influence big companies to set up research facilities here. Also due to the prevalence of a wide variety of diseases, which includes widespread cases of cancer and diabetes in India. These trials make way to the development of new drugs and trials are conducted on human subjects after the abundant satisfactory information has been collected on its quality and safety through various phases pre-clinical studies and needs an approval from the respective health and ethical authorities.

In light of such massive expansion of clinical trial labs in India, Clinical trial data management and statistical analysis is one such area that is growing rapidly, besides other related fields.

Among the very few training institutes in Pune that offer clinical research courses, CRB Tech Solutions Pune offers real time and focused clinical research training program. Our program is designed to transform Life Sciences graduates into efficient professionals who will add value to the companies who hire them. Our training course includes theories , internship, and development of soft skills that will increase your chances of employment, way ahead of your contemporaries.

You might find a few institute of clinical research that provide clinical research training in Pune but the need to take the right decision and follow the right institute in making a bright career.

Eligibility Requirements

Any one of the following minimum qualifications is eligible:

MBBS, BDS, BAMS, BHMS, B.PHARM, B.Sc. (Life sciences, Biotech, Nursing), Post Graduate Diploma

Mode of training

Class room training

  • 4 Months Job oriented Internship Program

  • Training and Internship in CR & CDM

  • Access to live projects in Pune

ENROLLMENT

Offered twice a year.

Payment options:

With credit card & debit card, payment options for fees is flexible.

What sets up apart?

• 100 % placement guarantee on paper

• We offer LOI (conditional offer letter) from our clients

• Unlimited placement calls for both alumni and freshers

• Known for best walk-in drives.

• Placement with lifetime support.

• Mentoring by very talented corporate expertise faculties.

• Train in German language and hence enhance your abroad prospects.

• Personality development training which will benefit you in developing soft skills hat would help you in cracking interviews which are very important in standing up among other contemporary candidates in competitions.

• 95% practically oriented training sessions.

• Good diagnostic Infrastructure and departmental infrastructure

A Training Program tailored for you:

• Detailed and expertise training is additionally offered alongside customized technical training to guarantee the general development of the students.

• Foremost curriculum: The modules of Clinical Research Training Program are upgraded and redesigned on a periodical basis by our industry expert.

• Guidance from professionals of the field

• Campus drives take place regularly: We have enlistment programs where a large number of our placement clients visit our organization, regularly.

• Aptitude training and interviews: Training in aptitude is a part of the syllabus as it enables you to successfully overcome the hardest of the aptitude tests, which you would face in the interviews. Mock interviews are taken to acquaint the students with real clinical research processes in ongoing research labs with an efficient study team, such that they can face real interviews with more confidence.

• Computer lab, course material, live projects?

Rules, and Regulations:

• Compulsory 90% classroom attendance.

• Proper dress code is a must in the class.

• Earn a support amount with no burden of fees.

Course Outline

Module 1

Preclinical Research

  • Drug Discovery & Development

  • Preformulation Studies

  • Formulation & Ingredients

  • Animal Research And Trials

  • Introduction to Clinical research

  • Introduction to pharmaceuticals

  • History of Clinical Research

Module 2

Clinical Research (core)

Clinical research process flow

  • Guidelines for Good clinical practice (GCP)

  • Essential documents

  • Preparation of IB

  • Preparation of Protocol,CRF,ICF

  • Quality Analysis in Clinical Research

    Bioethics and Clinical Research

    • How the ethics committee regulate

    • Pharmacovigilance

    • Regulatory affairs and regulatory submissions

    • Guidelines in clinical research

    • Career pathway in Clinical Research

    Module 3

    Clinical Data Management

    • Overview of Clinical Data Management

    • Overview of Electronic data Capture

    • Protocol Review

    • Data Management Plan

    • CRF Designing

    • Lab Data Handling

    • Database Designing and User Acceptance Testing

    • Medical Coding

    • I MedDRA

    • CD-9

    • Data Management Standards in Clinical Research – CDISC

    • Overview to Electronic Data Capture

    • Designing CRF in MS Word

    • Identifying disparities on CRF pages

    • How to generate queries for the sites

    Course for General Aptitude

    • Percentages Profit And Loss

    • Number System

    • Simple Interest Compound Interest

    • Permutation And Combination

    • Probability

    • Number Series

    • Coding Decoding

    • Blood Relation

    • Puzzle-Based Problems

    Clinical Research Certification

    Certification is presented to candidates only on successful completion of the course and after having paid all the dues with about 90% attendance.

    The management reserves the rights to change, delete, amend or modify its rules & regulations and schedules if a need arises and this will be applied to all the currently enrolled candidates in the ongoing program of Clinical Research Training.

    CRB Tech Solutions reserve the right to update the programs through changes in title, contents, and structure.

    There might be changes in the schedule, postponement and cancellations of the sessions conducted in classes.

    Register

    If you are interested please Apply now.

Related Topics:

1)Requirement of Clinical Research Associate

2)What is the responsibility of a clinical research associate?

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4 Trends Transforming Pharma Business

With changes occurring at a pace faster than innovations making their ways; adapting to changing circumstances is particularly essential to independent pharmacy owners, as pharmacy is sector in major transition. Knowing and acting on the following trends will help your business survives in this turbulent phases.

4 Trends Transforming Pharma Business

Medicare growth: As US population ages, serving Medicare beneficiaries becomes increasingly essential. In 2015, 42 million people were expected to be enrolled in a Medicare Part D plan. Seniors fill an average of 27.9 prescriptions annually at retail pharmacies; more than double the number of prescriptions for adults ages 19–64. More than a quarter of all prescriptions of the year 2014 were purchased through Medicare, and Medicare or Medicaid includes more than half of the prescriptions that an average independent pharmacy dispenses. Medicare will cover another 19.1 million people within 11 years. The serving seniors is increaClinical Researchsingly important, make the most of Open Enrolment season by marketing your pharmacy and helping seniors review their plan choices to make better decisions. And do not forget that new sets of seniors are entering the system throughout the year. Reach out to seniors in your community with events at senior centres and by building relationships with prescribers who may refer seniors to your pharmacy.

Explosion of preferred networks: In 2015, 87% of Medicare plans of Part D had preferred pharma networks, up from just 8% four years earlier. And, the criteria to participate in preferred pharmacy networks have changed; they now include performance on key quality measures. Participating in preferred networks is important in order to have access to Medicare patients. Failure to participate in preferred networks will limit a pharmacy’s access to Medicare beneficiaries in those plans. Though coClinical Researchnsumers have high satisfaction with their current pharmacy and pharmacies believe their customers are loyal, most Part D participants are likely to switch to in-network pharmacies. In fact, 85% of senior consumers say they would change pharmacies to save even $10 or less on a co-pay.5Maintaining participation in preferred networks requires constant vigilance of strong performance (in the top 20%) on key Star Ratings measures.

Prescriptions are negligible. For big pharma chains such as CVS and Rite Aid, prescription sales accounted for about 65–70% of revenue in 2014. BUt, in an average independent pharmacy, more than 90% of the revenue came from prescriptions, according to the 2014 NCPA Digest. Find other ways to serve your customers and generate revenues and profits, such as clinical services, front-end sales, new product lines and more. Independents are diversifying revenue streams, with 62% now offering immunizations, for example.8

Specialty medications will dominate drug spending. While fewer than 5% of people use specialty drugs, those medications comprise nearly a third of drug spending, and that is expected to rise to at least 50% by 2020. Although the bar for entering the specialty market can be high, partnerships offer a way for independents to use their unusual capabilities of high-touch care and bring into a significant revenue stream.

Whichever way you want to take your career you do; CRB Tech Solutions is here to guide you in your Clinical Research Career .

We conclude the discussion here. Stay connected with us this space for more discussions.

In the competition of many organizations CRB Tech Solutions developed a good name. It has earned a name in providing the best training in Clinical Research .

Clinical research jobs in Pune are increasing and to fulfill the current demand of the proficient candidates, you should consider enhancing yourself with our clinical research training program.

The Clinical Research review  by CRB Tech Solutions will guide you in considering a clinical research career in this field

Related Topics:

1)Requirement of Clinical Research Associate

2)What is the responsibility of a clinical research associate?

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Clinical Research for Health Checkups

Clinical Research for Health Checkups

Fit and Fine

The issue to be dealt is about the medicines which are reactive or which have side effects. If you fall sick or get some hurt or swelling you go to the doctor for check up and get some medicines if it is cured then no problem if not then it may lead or side effects. So this is all about such reactive medicines and either preventing disease or curing it at its first sight of symptom by Health Checkups.

“Respectable period for guest and medicine is only three days”

There is no possibility of everything being prevented but you can reduce the risk factor. Heart disease, for example, is the leading monster to end ones precious life in general. And the reason is inactivity, high blood cholesterol, obesity etc. But many people don’t realize the risks until they have a heart attack. We often ignore warning signs, and we don’t always get regular check-ups (sometimes because we can’t afford them). It is believed that within the next 10 years or so, wellness programs will be considered an integral part of most organizations for Health Checkups. They’ll even offer incentives for employees who participate and meet their goals and penalize those who don’t.

Health in your hands

Clinical-Research-for-Health-Checkups03

There is a prediction about how we take care of your health. Well there are various apps and gadgets for checkups say your blood pressure, Heart beat and technologies like scales that measure weight and body fat and send them via WiFi to a Web site, or an armband that measures blood pressure and plugs into an I-Phone, will be more common. So we will be sending such reports to reputed doctors who will be online receiving it any time at your service. Even there is a further advancement in future technology for health that silicon chips will be attached to your mirror in bathroom and when you blow into it your saliva droplets will let them know about your gene and whether you are in good health or not? It is an awesome Health Checkup scheme

Clinical-Research-for-Health-Checkups02silicon chip

Check your warranty

Well there are some diseases which are hereditary there might be a possibility or risk factor for you to get up with such disorders so if you want o have a checkup which will cost money and time the it will be hectic for you to deal with then so for this reason writing, getting your individual genetic code mapped costs around $100 to map your genes and place them on a CD. And it will be a part and parcel of your life. Your doctor will take a saliva or blood sample and almost instantaneously have a sort of owner’s manual for your body. Known as genomic medicine, this practice would allow doctors to both treat illnesses based on your genes and work to prevent you from getting sick in the first place.
Clinical-Research-for-Health-Checkups01

Related Topics:

1)Requirement of Clinical Research Associate

2)What is the responsibility of a clinical research associate?

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Clinical Trials

Clinical Trials

There is clinical trial opportunity provider which known as Select ClinicalTrials which provides you new research and opportunities for needy and increasing the medical zones and a disease proof vast for the patients. It is all about gathering datas abouty the common diseases and then providing home rememdies and details about the clinical trials as well and that’s what the website says about.

It allows those peole who interested to partifpaite in the clinical trials as a participant or as a volunteer for the trials and for the doctors and the therapeutic medicine. It also has online form filling the datils of those ho hoose to volunteer such as name of the participant, age and history of medical records and the trial they are undergoing currently and the procdess and the results of the trial. The target is not only for those who require improvements in health it is also for those people who are healthy enough as well.
image.png
It also shows the doctors incharge for the clinical trials and the particiapnts can gor through the clinical trial and then enrol themselves they can also search for associate clinical trials

It is said that the integral part of medical field is clinical trial. It also provides the details to the required participants and the acknowledgement for the investigators and the coordinators.

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How To Enhance Clinical Content Management

With the advancement of clinical research, clinical content management has become a priority and critical force towards success within quality-based reimbursement models.

How To Enhance Clinical Content Management

Health-care organizations are recognizing that leveraging technological infrastructures to deliver the most up-to-date clinical decision support to clinicians at the point of care is not only essential to meet regulatory requirements but also improve the outcomes and expenses.

Within any hospital’s greater CDS strategy, use of order sets has been identified by leading industry analysts as a key element for driving uptake of evidence-based practices and guiding clinicians to make the best decisions. The challenge is laying a framework for long-term viability of these tools as deployment, implementation and ongoing maintenance can be complex undertakings for the average resource-strapped healthcare organization.

While one notable hurdle to fully leveraging order sets is the ongoing maintenance activity required to keep content aligned with industry best practices, staying abreast of evolving regulatory guidelines for performance is equally challenging. Manual processes and workflows for identifying needed changes within a fluid regulatory landscape and rapidly advancing scientific field often result in compliance challenges and outdated evidence.

Rockford, III.-based Swedish American responded to these challenges by deploying a two-pronged strategy based on advanced clinical content management technology and governance. The health system comprises of a large care hospital unit, medical centre and comprehensive network of outpatient providers and clinics, has been able to significantly streamline order set review and editing by applying quality assessment to the front end instead of the back end of processes.

Identifying Opportunities

The SwedishAmerican fosters a culture of ongoing process improvement. The organization’s well-honed clinical content management infrastructure and governance model for maintaining order sets are an outgrowth of that culture and designed to lay a foundation for sustainability with CPOE and evidence-based practices.

As part of SwedishAmerican’s larger governance strategy, the clinical informatics team conducts reviews of the organization’s approximately 230 order sets to ensure compliance with industry best practices and national quality measures. Governance is built on three guiding principles: 1) always put the emphasis of the patient first, 2) clinical users play an integral role in clinical IT decisions; and 3) the IT decision process is standardized, transparent and responsive.

Until recently, a typical quality review process entailed meeting with clinical staff to review new evidence recommended through the comprehensive clinical content management system— ProVation Order Sets, powered by UpToDate Decision Support. Upon physician approval of edits and changes, content was forwarded to one of SwedishAmerican’s 7 quality analysts for review to ensure edits were done with quality initiatives. Revisions by quality reviewers were then sent back to the designated physician for reexamination.

A Good Strategy For Quality Review

Recognizing the significant resources required to keep order sets in synch with national quality measures, the SwedishAmerican clinical informatics team identified a strategy for streamlining the effort while also minimizing the potential for compliance gaps. It required that a quality assessment be applied to the front end of order set review rather than the back end by leveraging tools within the existing clinical content management infrastructure.

An automated system comprised of up-to-date national quality measures and customized rules is now used to conduct on-demand gap analyses of order sets and alert the clinical informatics team when content critical to quality measures is omitted or when content deviates from regulatory standards. As revisions are requested, compliance issues can be identified on the front end, eliminating the constraint that would previously occur.

When the new workflow and governance strategy was introduced, clinical informatics team leaders held an initial meeting with appropriate quality personnel to identify corresponding rules within abstracting methods for various national quality measures. The initial brainstorming proved beneficial as staff were able to identify opportunities to eliminate duplicated efforts between nursing and quality review. Staff also gained critical insight into the potential impacts of rules on clinical practice.

During the initial review of existing order sets, SwedishAmerican was encouraged to find that very few gaps existed with national quality measures—the most common associated with surgical care improvement project (SCIP) measures for preoperative patients. Overall the implementation of the new workflow has enhanced clinical practice, and staff is confident that measures align with regulatory initiatives and most important: patient care is optimized.

Whichever way you want to take your career you do; CRB Tech Solutions is here to guide you in your Clinical Research Career.

We conclude the discussion here. Stay connected with us this space for more discussions.

In the competition of many organizations CRB Tech Solutions developed a good name. It has earned a name in providing the best training in Clinical Research.

Clinical research jobs in Pune are increasing and to fulfill the current demand of the proficient candidates, you should consider enhancing yourself with our clinical research training program.

The Clinical Research review by CRB Tech Solutions will guide you in considering a clinical research career in this field

Related Topics:

1)Requirement of Clinical Research Associate

2)What is the responsibility of a clinical research associate?

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How To Ensure The Safety Of Medicines With A Pharmacovigilance Course

Before we get in details with Pharmacovigilance; let’s first know what it is. Pharmacovigilance, also known as “PV,” and it is the known as the science of collecting, supervising, researching, assessing and evaluating information from healthcare providers and patients on the serious effects of medications and treatments. 

The basic components of PV include a robust strategy which requires expertise in the following areas: medicine, regulatory, and technology. It involves the following main elements:

  • Strong processes
  • Case Study Report Capture and Processing
  • Literature Review
  • Signal Detection and Assessment
  • Risk Management
  • Periodic Safety Write-up
  • Safety Database

When must a manufacturer consider a PV plan?
Drug developers must consider their PV approach prior to human testing and in that duration of product development and the post marketing product lifecycle. 

What is the reason of studying PV?

  • Confers to the assessment of medicine effectiveness

  • Gives an effective communication to health professional and public.

  • Also gets involved in Medical and paramedical intervention

  • It helps to promote good understanding and education in PV

Before a nocel drug is launched in the market, a PG  Diploma in PV professional studies the safety measures taken before it hits the market to prevent adverse actions of the medicine. Public health has to be kept in priority when a medicine is released in the market. PV is also the scientific method of supervising, detecting, assessing and creating reports of the functionality of the drug in different patients with different medical conditions. Around the world, PV course is becoming very significant. The reason is that the industry is growing fast.

Need of PV

A constant pressure is there for the pharma industry to find the drugs that are sold all over the world to maximise profit in the shortest possible time. It is due to this some medicines will get tested for a short-term safety on a less number of selected individuals and that pre-marketing safety issues might get unnoticed. Hence it is necessary that progressing treatments are looked after for their effectiveness and more information are required about using of remedies in specific groups of population and combinations with other remedies.

Eligibility criteria

To find a career in this prospering sector with proper training in PV course; you have to enter the Course In PV, you must be a MBBS, BAMS, BHMS, BDS, Physiotherapy and occupational therapy graduates, BPharm, MPharm, Graduates and Postgraduates in Sciences, Botany, Life Sciences, Microbiology, Zoology, Biochemistry, Genetics and Biotechnology.

Course duration

The full time Course In PV is for two years though you can take over part time courses or online courses. The course timings would vary from one institute to another.

A lot of students are there who are feeling the urge to join these courses for a bright career ahead. Even you can opt for PV trainings from reputed organisations or institutes.

Whichever way you want to take your career you do; CRB Tech Solutions is here to guide you in your Clinical Research Career.

We conclude the discussion here. Stay connected with us this space for more discussions.

In the competition of many organizations CRB Tech Solutions developed a good name. It has earned a name in providing the best training in Clinical Research.

Clinical research jobs in Pune are increasing and to fulfill the current demand of the proficient candidates, you should consider enhancing yourself with our clinical research training program.

The Clinical Research review by CRB Tech Solutions will guide you in considering a clinical research career in this field

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Building Upon Trust With Patient-Cantered Care

The management of patient systems had become an increasingly arduous task for Memorial Hermann, and the marketing department wanted to bring all data into one easy-to-use system that could provide transparency by giving users a full view of patient acquisitions. The call centre also had a difficult time with the centralized management of all events, and sought to improve efficiencies by having a single source for all event-related information, including details on future events.

In addition, TIRR Memorial Hermann is offering inpatient and outpatient rehabilitation following traumatic injury, required to streamline it’s on board process of new patients for both inpatient and outpatient care into one common system, increasing uniformity and standardization. 

Improving Patient Outreach and Management

Memorial Hermann wanted a common system that would manage marketing outreach and patient acquisition, event management and registration, call centre functions, and TIRR Memorial Hermann inpatient and outpatient tracking.

Perficient implemented Microsoft Dynamics CRM. Our methodology for implementing CRM systems is based on proven industry best practices and standards and has the following:

  • Inception, where requirements are gathered
  • Elaboration, that includes installation and to validate the system
  • Construction, or the making and deploying phase
  • Transition, which includes training, launching, supervising, and supporting the new system

Perficient led Memorial Hermann via strategy sessions, design iterations, and solution architecture sessions to make sure both business partner and executive support.

There were 4 parts to the initial roll-out of Dynamics:

MARKETING

The new marketing strategy and patient management system blends into the existing enterprise content management system and allows capturing information of interested people and then streamlining to the appropriate internal resources. They developed the new patient acquisition solution to provide the ability to actively track correspondences and report on activities. The innovative design helps users to make it an integral part of their daily activities.

EVENT MANAGEMENT

Perficient installed Eventix, an event management system. This complete module is designed to work with Dynamics CRM and includes registration, invoicing, and payment tracking. 

CALL CENTER

They utilized the Service module of Dynamics CRM to implement the ticketing functionality. Memorial Hermann provided Perficient with detailed requirements to effectively install the ticket management system in support of the organization’s processes

INPATIENT AND OUTPATIENT TRACKING

TIRR Memorial Hermann needed a central location to function as the communication center for its solution hub. This involved automating the referral process as required, along with workflow automation. By automating it’s on boarding process with its management software, the solution centre team has a technology to efficiently manage the process, greatly improve communication regarding the progress of referrals, and attain essential business intelligence about referral sources.

A CRM System

Perficient oferred both administrative and end user training, teaching best practices and ensuring users have the tools and resources to successfully utilize the system moving forward. Following an implementation, Memorial Hermann is leveraging Microsoft Dynamics CRM on-premises to handle community outreach, call centre management, and specialty patient on boarding. Future plans might include adding other departments within the organization, like home health and insurance. A cloud-based solution be required in the future, Dynamics CRM has BAA availability to address HIPAA compliance. 

  • Improved community reach enhances the number of new patients by attracting, involving and track prospective patient interactions
  • Specialty group on boarding process automates the process of bringing rehab patients into the system for both inpatient and outpatient tracking
  • Call canter technology upgrades an older, stand-alone system to a connected CRM system that enables the hospital to track inquiries concerning events and patient referrals via the phone and onlineClinical research jobs in Pune
  • Improved customer engagement across the organization

Whichever way you want to take your career you do; CRB Tech Solutions is here to guide you in your Clinical Research Career.

We conclude the discussion here. Stay connected with us this space for more discussions.

In the competition of many organizations CRB Tech Solutions developed a good name. It has earned a name in providing the best training in Clinical Research.

Clinical research jobs in Pune are increasing and to fulfill the current demand of the proficient candidates, you should consider enhancing yourself with our clinical research training program.

The Clinical Research review by CRB Tech Solutions will guide you in considering a clinical research career in this field

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2)Top 10 Clinical Research Interview Questions

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How Clinical Research Management Can Help You?

A scientific analysis manager conducts analysis, investigations and tests of protocol subjects and participants. Their responsibilities consist of collecting data and monitoring the results of the scientific tests. Clinical analysis planners also collaborate with other medical managers in the implementation of scientific tests and the recruitment process of medical trial participants.

Work Experience

To become a scientific analysis manager, applicants for these positions should have prior encounter as scientific analysis experts. Understanding the scientific analysis process and participating in scientific tests are important attributes that companies may need applicants for the job to have. The degree of scientific analysis encounter needed to qualify for a job as a scientific analysis manager is determined by the companies. Some companies may need only one to two years of scientific analysis encounter, while other companies pursue individuals with additional years of encounter.

College Education

Many companies may seek applicants for the scientific analysis manager place who possess an associate’s or bachelor’s degree in scientific analysis. Having a degree in scientific analysis, coupled with less than one to two years of expertise in scientific analysis, may meet adequate minimum qualifications with some companies.

Because scientific analysis planners prioritize and oversee the development and implementation of scientific analysis tests, many companies need them to be licensed as a registered nurse or a licensed practical nurse. Many companies who seek applicants with an RN or LPN license may also need them to have at least one year or more nursing expertise in a medical facility.

Certification

Certification also benefits applicants for scientific analysis manager positions, and some companies need applicants to have a documentation in scientific analysis from approved organizations that offer documentation courses and examinations. The Society of Clinical Research Associates and the Association of Clinical Research Professionals are nationally recognized organizations that offer documentation programs for scientific analysis experts.

Additional Qualifications

Many companies need individuals to be proficient with Microsoft Word, Excel and Outlook. Interpersonal communication skills and encounter working in a team environment are skills needed for this job place. Strong organization and prioritization skills are also beneficial skills that companies may need applicants to possess for the scientific analysis manager place.

Supervisory Role

Many scientific analysis experts become promoted or advance to the higher level supervisory positions after gaining additional qualifications and expertise in scientific analysis. Clinical analysis planners oversee the entire process of scientific analysis investigation and tests and ensure that all medical experiments and tests are compliant with the objectives of each project. Clinical research management is a wonderful field and you can choose to make your career in this field.

Related Posts:

1)6 Ways ResearchKit Would Change Clinical Research

2)Top 10 Clinical Research Interview Questions

Don't be shellfish...Digg thisEmail this to someoneShare on FacebookShare on Google+Buffer this pagePin on PinterestShare on LinkedInShare on RedditPrint this pageShare on StumbleUponShare on TumblrTweet about this on Twitter