Tag Archives: clinical rersearch courses in pune

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

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What Are the Steps Related to Clinical Assessments?

Clinical assessments are a type of analysis that involve huge numbers of individuals order to test new therapies. Many, but not all analysis, are assessments.

Clinical analysis aim to find out important info in response to any adverse wellness question in a very methodical way. A well designed analysis will provide efficient evidence that can help improve NHS services and therapies and the healthcare understanding of doctors.

To be efficient it usually involves obtaining wellness details from a variety of individuals whose healthcare concerns fit the topic of the study. Where sufferers agree, or “consent”, to join as volunteers, this details might be obtained by:

  • Interviews
  • Questionnaires
  • Tests on sufferers in a healthcare setting that measure the effects of new drugs
  • Using individual records
  • A combination of the above

If you are interested in becoming a individual in research:

You could ask your GP or Advisor to consider any assessments or analysis that you may be suitable for You could check out the web pages for your local Clinical Research Network

You could check out the The UK Clinical Trials Entrance which provides details about scientific analysis assessments running in the UK

The NHS Structure says that your NHS healthcare professional should inform you of any analysis for which you may be eligible. ‘Eligible’ here concerns how you fit the strict healthcare and personal requirements used in the study design for it to work technically.

Think about it for a time that you are a effective psycho therapist. Cynthia comes to see you because she’s having a problem. How do you cure her? How do you even know incorrect with her?

Clinical assessment is a way of identifying and preparing treatment for a individual that includes analyzing someone in order to determine incorrect. There are several kinds of emotional tests, all of which have their own pros and cons.

What’s the point of assessment? To response that, let’s go back to the time that Cynthia walking into your workplace. She informs you that she’s sensation very pressured out and nervous because she keeps failing to remember factors. She used to be really up to the mark, but lately she has problems keeping in mind where she sitting her car or what she did just a couple of moments ago.

What’s incorrect with Cynthia? There are several factors that can cause forgetfulness. The only way that you can find out incorrect with her is to do some kind of assessment. Medical tests help you, the psycho therapist, to know what might be resulting in trouble for your individual. Clinical assessment example can be related to psychology.

Related Topics:

1)Requirement of Clinical Research Associate

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

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Pain Management Trials With The Placebos

Pain Management Trials With The Placebos

Going by the definition of placebo, it is an inert substance that has no effect on our body. In clinical research, placebos such as sugar pills are used as controls against which the effects of experimental drugs are measured.

Even though the placebo-effect has become a well-recognized phenomenon. A phenomena in which a patient believes he is being administered an actual drug and gradually improves in spite of receiving no active substance.

It also works with surgical procedures. Just like drugs, placebo or sham surgery is shown to produce results that are equal to actual surgery, though the physical problem is not addressed.

Since years, we’ve known about the “placebo effect”—that a patient, simply by believing that a treatment is effective, might experience a beneficial effect from a clinically ineffectual treatment. Of course, it goes against the ethics. The ethics of deceiving patients into falsely believing that a placebo is an effective treatment is questionable—so clinical researchers have recently turned their attention towards open-label placebos.

Random Controlled Study:

OLP vs TAU Group

A recent Pain article documented a randomized controlled study of open-label placebo treatment for chronic lower back pain. 97 patients were divided into 2 groups: One continued treatment as convention (TAU), while the other group received open-label placebo pills (OLP). Before starting with the study, patients were told that the human body can automatically and powerfully respond to taking placebo pills—and all patients were aware of whether they were in the TAU or the OLP group.

At the completion of the study, patients in the OLP group showed significant decline in both pain and disability—in simple words, though they knew that they were on a placebo pill, the patients yet reported an improvement in their chronic lower back pain.

But what does that mean for central nervous system (CNS) clinical trials?

The Essence of Rater Training in Clinical Trials

In this study, the efficiency of the placebo pill can largely be chalked up to the nurturing approach of the rater and investigator, who repeatedly stressed the positive potential of the placebo effect. In CNS trials—especially when it comes to pain management—rater training is absolutely essential to avoid the increasing placebo response rate.

Solution: A Supportive Environment for Treatment

That’s why Clinical Trials employs a four-stage certification process for raters, validating their experience and knowledge and calibrating them to the standard scoring conventions and protocol specific study criteria at the beginning of each study. Raters require knowing that simply being in a therapeutic environment can heighten placebo effect—so a “research” atmosphere, rather than a “therapeutic” one, must be the goal. Interaction with site staff must be controlled, and not unintentionally create a non-specific supportive treatment environment. Staff also must know that they should have no expectations of drug response, either positive or negative, and should explain the same to the patients.

How Rater Training Can Benefit Pain Management Treatments?

To mention, the placebo effect is not a replacement for effective pain-management treatments. By properly training raters to be well aware of the placebo effect and assess each participant in CNS clinical trials, they can very effectively continue the search for treatments for low back pain, osteo-arthritic pain, neuropathic pain and other areas of CNS expertise.

We conclude the discussion here.

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 meet 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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Interview For Pharma Freshers : Tips & Preparations

Interview For Pharma Freshers : Tips & Preparations

Today we write this blog topic keeping in mind the Phrama candidates who are seeking job and the trouble they find in preparing and coming out bright in respective interviews.

Let us share a secret! Yessss Here if studies to be believed then most of the interviewers were never trained before to conduct interviews. Even the managers are anxious, confused and stressed like the job seekers. This blog will help you in directing how to avoid from being into stressful situations before an interview.

What are the pharma companies and the CROs are looking for?

  • Your confidence
  • How you play in a team
  • How you focus and pay attention to minute details
  • How good you in handling the most difficult questions
  • You attitude and body language.
  • How you manage stress

Do’s and don’ts before attending interview

Do research about the interviewing pharma company or CRO?

  • Main areas where they work.
  • How your skills match with the company’s area of work

Punctuality and discipline

They are the key factors that decide candidate’s fate. Never be late for the interview, be there ahead of time.

First impression matters

Take advantage of this view and no matter how anxious you are, wear a smile that will show how confident you are and your self-esteem. Another reason to keep smiling because research says that people who smiles don’t get stressed.

Handshake

A firm handshake with interviewer is a must, by using the whole hand. Don’t be loose or too tough at the hand shake, either has negative message, so be casual an firm with confidence.

Attitude

The moment you enter the interview room, simply don’t go and sit down. Wait for a few seconds until the interviewer tells you to have a chair. If the interviewer doesn’t offer, then ask politely if you could sit down. Do not put anything on the interviewer’s desk

Interview questions

All interview questions are not the same. So you need to answer as they come. Some question needs precise answer and a few needs elaboration.

To mention there are 4 types of questions:

Straightforward questions

  • Tell us about yourself.
  • What are your strengths?
  • What accomplishments your are proud of?
  • What of your skills you have that would be good for this company?
  • Why should we hire you?

Questions behind questions

  • What do you know about this company?
  • Where do you see yourself 5 years from now?
  • Why you left your last job?

Stress questions

  • Tell us about your greatest failure
  • Tell us about your greatest weakness

Questions you need to or can ask the employer

  • What is the ideal candidate for this profile?
  • What would be my role in the first year of employment?
  • What are the company’s new products or services that is going to launch?
  • What do you like about working at the company?
  • Can you suggest how I can personally contribute to drive this business to the competitive edge?

We conclude the discussion now. What we discussed are only a few questions that might come your way. You have to prepare your own notes for the above mentioned questions and crack your interview confidently. Good luck!

To be contd.

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 meet the current demand of the proficient candidates, you should consider improving 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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21 Trends for Nurse Practitioners in 2016 Part III

21 Trends for Nurse Practitioners in 2016 Part III

Today we continue with this blog topic we started and conclude the discussion that we started a few days back, what is making nurse practitioners trending in 2016.

Population Health

The term maninly includes geographic populations such as communities or countries but could also be ethnic groups. The actual goal of population health initiatives is to understand that every group has a unique need and create target friendly interventions to look into the needs. If reports are to believe then this collaboration is really being fruitful and significant.dicalechnolog

Electronic Medical Records (EMR)

A report stated that by December 2015, the EMR market was estimated to be worth $23 billion with more than 400 unique vendors. The report made the top earning EMR companies happy,but clinicians were not.

In 2016, the EMR market players might shrink. With the need of smaller medical practices those practices will take upon the larger organization’s EMR. This attempt by healthcare groups will gradually squeeze out smaller EMR vendors, and the market will incline more towards the EMR giants like Epic and Cerner.

Mobile Health(mHealth)

mHealth is a rising trend currently in health sector. Sometimes called connected health, it is defined as the generation, aggregation, and dissemination of health information via mobile devices.Other trends in the mobile health market include anthe alternate utility of helpful smartphone apps. To mention, health and fitness apps grew 87% faster than the overall app industry in 2014. This rise has attracted major technology companies like Apple and Google to introduce their own mobile health products.

The Cloud

As per an international survey, 83% of healthcare officials are currently using cloud services for human resources applications,clinical information and disaster recovery. Practically cloud-based softwares in healthcare lessen the costs by limiting number of servers a hospital needs to purchase.

A huge challenge in clinical trials has been data storage and currently, 30% of the world’s computer capacity is used to archive medical images including CT scans, x-rays and angiograms. Cloud helps maintain data with an exponential capacity throughout the entire lives.

Telemedicine

Currently with an attempt of digitalization and increased public access to WiFi, and a essence of connectivity, telemedicine is fast emerging another booming industry in healthcare technology. Repots suggest that telemedicine is safe and cost effective.

Ingestibles, Implantables, & Sensors

In the years 2014 and 2015 health technology wearables made rounds in headlines, and this year it took to more about ingestibles, implantables, and sensors. Google recently announced their smart contact lenses that can monitors a wearer’s blood sugar levels in real time.

Decision Support

Yes we shall mention aboyt IBM’s Watson, named after the company’s first CEO, it is a highly intelligent computer capable of answering complex questions using natural language processing. It is to believe that the future for Watson Health is bright.

The Internet of Things

As it relates to the healthcare sector, it attracted a lot of attention in 2015 when Market Research reported and predicted that this industry would be worth $117 billion by 2020. Abbreviated as IoT, is said to have all objects connected and collects data. The value of IoT can be ascertained from the correlation between all the things and the data created by them.

The IoT helps nurse practitioners to allow theirs patient’s to recover at home yet keeping a watch ober them and monitoring their health status from a distance making use of products like BodyGuardian Remote Monitoring System.

Now we conclude here. Hope the discussion is giving the right and precise information to you.

Stay connected with us for more discussions to come. Let us know your experience with us in the comment sections below.

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 meet 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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How Scalable Is Your Clinical Trial Payments System

How Scalable Is Your Clinical Trial Payments System

Today in this blog topic we shall discuss about ClinPay a payment solution initiated by Bioclinica and is being very helpful to the Clinical Research Organisations worldwide.

How Scalable Is Your Clinical Trial Payments System

Bioclinica came up with this alternate payment option to help CROs that have outgrown their site payment systems. Whether they’re using manual home-grown system or spreadsheets with the increase in number of clinical trials they’re conducting, the CROs often find it difficult and a realisation that the current systems are not sufficient.

It is very important to maintain accurate and timely payments and as a result, it’s important to choose a payments solution that is scalable, in other words it should be an automatic one as opposed to the manual. ClinPay is a part of the suite of Bioclinica products designed to automate the entire financial lifecycle of global clinical trials, which includes contract management, contract term translation, payments, accounting and reporting functionality. ClinPay can significantly reduce workload and operational costs, make an access to clinical research payment information, and enable multi-currency management. To mention that ClinPay is very much data-driven and automatically evaluates incoming data against contract terms in order to determine a wide variety of payments, which says that no matter how vast your study is, how many sites you possess or how you payment terms, ClinPay can scale to fit your needs.

Let’s share an example for a big CRO who has found success after switching from the manual system to an automated. A top CRO grew significantly within a span of short period of time, making the investigator payments process a significant and admin-intensive challenge. To mention the 100 team members were given the task to hand just grant payments. The CRO does 350 to 400 global trials at a given time, and hence was becoming difficult to make payments to sites in time and in accurate ways. As a result, the CRO was flown with complaint mails and messages from sites about payments, which lead to bad relationships with the sites as well as sponsors. The CRO realised that their manual payments model wasn’t automatic, and they needed to do the technology way and find a technical solution to keep pace with their growth.

After discussing and reviewing many good financial management solutions, the CRO decided to give ClinPay a try because it was the only end-to-end solution that could manage all the unique challenges and characteristics of a clinical process. The CRO was also particularly interested in ClinPay’s ability to make global payments and knowing of country-specific requirements. Additionally, the CRO wanted to use ClinPay to pay their sites accurately and on time as well as achieve a significant amount of financial savings. Finally, the CRO wanted to use ClinPay to enhance efficiency with their clinical research team so that team members could focus more on the trials and less on site payments.

Now the story is that by using ClinPay, the CRO has well organised their process, gained remarkable efficiencies and allowed many of their team members to focus on more vital tasks.

We conclude.

Please let us know your opinion in comment section below. Readers’ opinions are valuable! A good discussion is the gateway to many innovations and ideas.

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 meet 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 Posts:

1) Why Clinical Trials Are Very Much Useful Through Mobiles?

2) Clinical Trials and Its 4 Stages for New Medications

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Changes Required In Clinical Trial Of Alzheimers Disease

Changes Required In Clinical Trial Of Alzheimer’s Disease.
Changes Required In Clinical Trial Of Alzheimers DiseaseToday’s blog topic is about rectifying screen failure and enhancing recruitment rates in clinical trials of Alzheimer’s Disease.

Failures in Alzheimer’s Disease (AD) clinical research have many factors which includes an inadequate understanding of mechanisms of action and poor target engagement; poor study design, wrong stage of AD matched to a particular drug, limited statistical power of endpoint measures, and inclusion of ineligible participants, also contribute.

Proper approach to study design and optimization of recruitment/screen failure rates are proving increasingly significant as the field focuses on putative disease-modifying agents and patients that are early in the disease spectrum.

Studies of patient eligibility found that only 10–27% of potential participants are trial-eligible. That is really a lees count. To mention, few AD patients are aware of research opportunities and many are unable or not willing to take role. Many aged people lives alone and might not have access to a caregiver who can help them in participation.

Truly speaking what is imperative to success of an AD trial is not one but two participants, i.e. the patient and a study partner, and the involvement of this dyad is essential.

To choose the right patient for a study and exactly translating their medical data into a protocol-specific entry criteria, stirs major challenges. Other hurdles include medical co morbidities, use of prescribed and OTC medications, and behavioural complications which could all be exclusive.

Improving Screen Failure For AD Clinical Research

The development of symptomatic treatment in mild to moderate AD fals between the ranges of 15-35%. This range is manageable, but very common for trials to fail twice the rates in early AD populations. To overcome these, a gradual approach to patient’s eligibility factors might be utilized, that takes into account all known and estimated screening variables.

It is quite difficult to lower failure rates caused by unpredictable factors like amyloid level on CSF, safety brain MRI indicating ARIA and amyloid-PET.

One promising technique utilizes statistical tools that predict the presence of amyloid/tau or even the eventual diagnostic conversion to AD. Conventional techniques that involve using multiple regression analyses to predict the presence or absence of beta amyloid or tau on imaging or in CSF, based on scores on previously obtained and easy to acquire screening measures such as cognitive test scores, demographics,genetic status, clinical signs/symptoms and structural MRI findings.

Another method has been suggested to minimize the clinical trial costs without making compromising with statistical power. Utilizing an adaptive design for data acquisition exploits harmonic analysis of a band-limited signal graphically, whose node corresponds to participants with the goal of fully recovering a multivariate signal on the nodes, given the full set of lower-cost features and a partial set of more expensive measurements.

Analytical techniques offer the opportunity to predict which subjects will qualify for study participation in an adaptive manner, with each additional piece of screening information enhances the success of final predictions based on biomarkers. These methods and an increased familiarity of patient clinical status and the use of a hierarchical approach to screening should help to reduce screen failure rates, improving overall recruitment rates in these notoriously difficult-to-enrol trials.

We conclude here.

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 meet 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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How To Get The Right Patient In Making A Decision

How To Get The Right Patient In Making A Decision

With the rise of clinical trials all over the world, there is an increased involvement of patients in medical discussions, a very welcoming policy or methodology. They have rights, not only since they are the ultimate customers but they are every essential to the entire process. Their views can help in the regulatory process, with its raising sacle of interactions like patient representatives in some of its scientific assessment of individual products.

It is a two-way path, too. For every soul concerned in healthcare sector, an informed patient can help and support make care more effective, with improved support, more developed relations with respective physicians, and wider broader understanding of the challenges of drug designing and regulation.

But this two-way path can also prove to be dangerous. Patient’s opinions and demands might not always share the logic of the process that produces their products. It is quite reasonable to seek passenger’s views on the attribute of aircraft seats, but they have quite less to contribute on airframe design or navigation. In similar ways, not every view of every patient is could be helpful in determining the most appropriate scientific, clinical or commercial approach to medicines. An wrongly informed patient can make a doctor’s life pathetic.

So how can you strike the right balance into customer links and decision-making on remedies? A European project that began at the end of October is aiming to take over this hurdle. The final outcome would be suggestions to support developing guidelines for industry and health technology assessment authorities. In simple words when and how should decision makers give an ear to the patients?

The project, sponsored by EU’s joint-venture in drug research, would mainly concentrate on three disease areas where patient and clinical trial partners have expertise: neuromuscular disorders, rheumatoid arthritis and cancer.

According to Ulrik Kihlbom, one of the Swedish academics involved in the above mentioned project, the challenge is very real and needs a thorough discussion among a wide range of partners. How could a settlement authority weigh the patient perspective against cost-effectiveness when making a repayment of money decision, he reviews? Or how does a regulatory authority weigh patient need contrary to safety matters? Patient’s views need to represent the actual opinions patients have, and be unbiased. And for the individual customer, at what point should his or her voice be listened to? When his or her first diagnosis occurred, or when was under treatment? It is recommended that the patient’s choice will definitely change during the occurrence of illness. Is it to know when your choice is such that your physician must listen to them?

At this present time in Europe, patients’ voices are being increasingly given attention on concerns as wide as access to social and health care, availability of medicines, assessment of health technology and the shaping of broad health policy, the preferable initiative is quite in time. The very question, however, is whether Europe can wait for more years for its recommendations, as “patient potential” is already coming up very strongly, whether it is “correct” or wrong.

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

With increasing Clinical research   there is an immense need to meet the current requirement of the efficient candidates, you must consider improving yourself with our clinical research training program.

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

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Being Human to NGOs and Inhuman to Drug Research

Being Human to NGOs and Inhuman to Drug Research

The clinical research sector since the year 2005 has been expected to grow in double digits due of its vast patient population. But a key question on being human or inhuman with investors, analysts and all stakeholders who have been observing this market in the recent times.

But things have not been good for the industry particularly since 2010.

The data available at the Clinical trial registry of India has been witnessing a step hike in the registrations since it came into inception.

Owing to some unavoidable circumstances, defects in clinical research practices came to light in a hospital based trial in a metro city in India in 2011. This happened despite the fact that the trial was registered at all major sites and was being done by a popular pharma company. The matter came into notice when an NGO filed a petition in the Supreme Court in protest against possible anomalies in their practices. Seeing the same, the Supreme court issued an order to the Indian drug regulator to outline strict laws to conduct clinical researches in India increasing concerns with respect to Ethics and Ethics Committees, safety of volunteers, informed consent matters and volunteer compensation in case of adverse events. Based on the same, a committee was formed to present before the parliament its advice. The words of the committee were brought to the notice of the regulators and the industry leaders for their further action and comments.

Anyways the Supreme Court placed an order on the 30 September 2013 that no clinical trials can be approved till the laws are followed.

This news was published in major newspapers in India. In the current scenario, the Indian regulator cannot approve clinical trials even if the same are in view of public interest. This decision that came from the Supreme Court is expected to expedite the rule formation process. However it is difficult to say in the present times as what will be the impact of the Supreme Court order. According to the key industry leaders, an impact as a consequence would be that it is likely to take away the clinical research practice away from India.

In the name of ethics, a lot of suffering is about to fall on the world of novel drug research. Novel drug research is heavily dependent on outsourced clinical research and people will continue to suffer and die of incurable diseases. Some believes that humanity will be at stake if the law makers continue to support “only humanity”. Little do they realize that the future of humanity is at stake as “unknown” disease continue to lurk the human population.

Clinical study reports explain every aspect of the clinical trial for a novel drug, including the number of participants, methods, analysis, and conclusions. Releasing this data is a huge step in the very competitive and too secretive pharma industry, it is researchers, health care providers, and patients who stand to gain.

Either way, these test subjects came volunteering for these programs, freedom over own body etc. True, there is a chance that test subjects stand to see their health improve. But when people register to participate in drug trials, they are signing up for a casual game of Russian roulette with their health; the stakes are high.

Hope you liked this perspective on clinical research.

Among the many competition of organizations, CRB Tech Solutions developed a big name. Its better known in giving the best training in Clinical Research.

Clinical research jobs are increasing and to meet the increasing requirement of the highly able professionals , you should consider improving yourself with our clinical research training program.

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

Related Topics:

1) How Does Clinical Data Matter?

2) What Mobile Should Mean For Health Care Part 1

 

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Digital Health

With digitalization is its development, the field of clinical research introduces a new word to the list. Yes we are talking about Digital health which is the way by which digital and genomic revolutions converging with healthcare and society. Digital health is enabling people to a better track and improve their own and family’s health, live a better life, more productive lives and improve the society.

Now what is the scope of digital health? It has a broad scope that includes health information technology (IT), mobile health (mHealth), wearable devices, telemedicine and telehealth and also personalized medicine.

Other usage of digital health in their efforts to:

  • Lessen inefficiencies,
  • Enhance access,
  • Lessen costs,
  • Improve quality,
  • Make personalized medicine for patients.

Patients and consumers can use digital health to manage and keep a track of their health and wellness related activities.

The use of technologies such as social networks, smart phones and internet applications is not only changing the way we communicate, but is also providing novel ways for us to supervise our health and well-being and giving us greater access to information.

Why is FDA focusing on Digital Health?

Many medical devices now have the ability to connect to and communicate with other systems or devices . FDA approved devices are are being updated to add digital features. New devices that already have these capabilities are now explored.

Many stakeholders are involved in digital health activities, including patients, researchers, health care practitioners, conventional medical device industry firms, and firms new to FDA regulatory requirements, such as mobile application developers.

FDA’s Center for Devices and Radiological Health is overwhelmed about these developments and the combining of medical devices with connectivity and consumer technology. The following are the topics in the field of digital health on which the FDA has been working to provide clarity using practical approaches that balance benefits and risks:

  • Mobile medical apps
  • Wireless Medical Devices
  • Health IT
  • Telemedicine
  • Medical Device Data Systems
  • Medical device Interoperability
  • Software as a Medical Device (SaMD)
  • General Wellness
  • Cybersecurity

How is the FDA developing Digital Health?

CDRH has established the Digital Health Program which tends to protect and promote public health and provide continuous regulatory clarity by:

  • Encouraging collaborations and increasing outreach to digital health customers.
  • Creating and implementing strategies and policies for digital health technologies.

Federal Trade Commission Mobile Health Apps Interactive Tool

If you are designing a mobile health app that collects, creates, or shares consumer information, click on the button to take you to the tool on Federal Trade Commission’s website to find out when FDA, FTC or Office of Civil Rights (OCR) laws apply:

Genomics and Genetics

According to J. Craig Venter, digital health is basically a DNA-driven software device and there is no difference between digital code and genetic code. Digital code is a binary code: 0, 1. while, genetic code is a four-base code: A, C, G, T. There can be no conversion between the two as well as digitized man, as Topol defines it in expanded terms.

Stay connected for more exciting blogs and articles and increase your knowledge with us.

Are you looking for Clinical research course in Pune, then our CRB Tech Solutions would provide with help and support. Its very popular in offering the best training in Clinical Research.

Clinical research jobs are pacing and to meet the emerging need of efficient professionals , you should consider upskill yourself with our institute of clinical research.

Clinical Research review by CRB Tech Solutions can help you in considering a clinical research career in this field.

1)5 Ways ResearchKit Is Revolutionizing Clinical Research

2)Crowd funding In Clinical Research

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