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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

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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.
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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.
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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 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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First in Human (FIH) Clinical Trials

First in Human (FIH) Clinical Trials

First this first, you must know what FIH is as all FIH trials are not the same. FIH trials are basically conducted with 20-80 study volunteers. The objective is to find the metabolism and pharmacologic action of a test drug in humans, the side effects that might be associated with increasing doses, and if possible gain early evidence on effectiveness.

In simple terms, FIH studies give researchers a base to understand the safety of the drug and might also show the action mechanism in humans.

Not an easy job

Nothing is so easy, there is Phase I studies that deviate from the FIH Phase I cookie-cutter norm, such as:

  • Clinical trials in which volunteers receive one of the following types of test drugs:
    1. A new compound in a novel drug class

    2. A novel compound in a drug class that is being through human testing with a different IND

    3. A novel drug/approved drug combo

    4. An approved drug with a novel formulation or changed dose

  • Clinical research requires a special population of age or type.
  • Clinical trials for which the drug is therapeutic

Each FIH trial should be evaluated on an individual basis because the objectives and risk factors vary. The preclinical data, trial design, proposed population, and safety measures must be evaluated for every FIH trial.

What part does the CRO play?

The CRO plays a vital role. They are to offer their expertise to make sure the successful completion of the clinical trial.  

CROs experienced in the conduct of FIH studies are knowledgeable and equipped to guide sponsors through the process of designing the best possible protocol. They conduct studies for the whole day, starting from Monday to Sunday. They would tell you about recruitment, if your blood draw times are feasible, and if your timelines are realistic.

A team with general or late phase clinical research expertise is not sufficient.

It is essential that the Chief Investigator and the study team have a lot of experience conducting FIH trials and possess the qualifications to make sure that the trials go smoothly. The clinical team is vital in ensuring that the protocol is optimal with little scope for amendments or deviation, while also making sure recruitment goals can be met, even with the most strict inclusion/exclusion criteria. Whether it’s a simple Single Ascending Dose (SAD) trial or a complex, adaptive design, the team conducting the study is a pivotal factor to success.

When it’s time to outsource a clinical trial to a CRO, it’s best to find out how involved the principal investigator (PI) and sub-investigators will be. Moreover, the experience of project managers, study coordinators, lab personnel, data managers, and medical writers are equally important. The PI is responsible for supervising the staff; however, problems can arise when a PI is either an inexperienced or uninformed in conducting FIH trials or puts too much responsibility on the staff to perform tasks that the PI should be overseeing.

In short, an experienced CRO can minimize the risk of recruitment and retention issues look after the safety concerns, bad data and a whole list of other issues that could halt your FIH clinical trial.

Does your CRO have what it takes?

You need to look into the matters discussed above and have your words with your consultant to know hoe efficient your CRO is.

We conclude the discussion here.

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

Clinical research jobs in Pune are increasing and to meet the current requirement 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 Industry’s Strategy to Epidemics

Clinical Research Industry’s Strategy to Epidemics

In the field of clinical research mainly epidemic response face many challenges. Clinical research done on global health concerns often needs rapid action, immediate trial start-up and lower standard good clinical practice (GCP), among many other struggles. It’s very difficult to carry out a clinical trial during the course of an epidemic. However, there are measures to overcome these challenges.

In a recent conference of Partnerships in Clinical Trials (PCT) that was held as a part of Boston Biotech Week (BWB), two inspiring presenters shared their story of journeys working to combat infectious diseases, like Ebola and Zika, in 3rd world countries. Both the presenters presented a common idea that the research industry needs to work together to become more prepared for responding an epidemic occurrence of an outbreak.

Collection of right data

Presenter Toni Hoover of Bill & Melinda Gates Foundation said on the power of technology and therapeutic innovations to fight diseases that affects underprivileged individuals. She said that their organization is dedicated to enhancing quality of life worldwide, works with many people to give vaccines and new therapies to people in poor and downtroden communities.

The Foundation and its collaborators in the biotech field are working to collect data required to make informed decisions during an epidemic. Hoover said that the data has the potential to be utilised to predict where the next epidemic might occur, pronouncing that the whole healthcare ecosystem needs to work together to prepare and develop a platform for combatting with epidemics like that of Ebola and Zika. She said that Zika is a perfect example that says the need to think about interventions, but also how preparations can be made with the help of collection of the right data to advice decisions.

Industry transparency must be increased

In the same manner, presenter Trudie Lang of the Global Health Network at the University of Oxford expressed her belief that the clinical research industry must be more prepared to respond in the event of an outbreak.

With reference, Lang shared her experience as a researcher performing an Ebola trial in West Africa. She described the hurry to begin the study and was under immense pressure to complete the trial in 16 week only. Lang said that her team was able to complete the clinical trial at rapid speed, but admitted they were too late. The epidemic already spread fast by the time the trial was complete.

This experience made Lang realise that the research community must be always ready to combat infectious diseases before an epidemic reaches a downward slope, more possibly before an outbreak occurs.

Finally Lang proposed a solution to the current problem by saying that research information must be shared and there should be transparency in clinical research industry.Lang came forward with an argument that sharing clinical research information between groups, plagued areas and regions would enhance the agility of a research enabling faster response to life-threatening diseases.

Fact is that epidemics and global diseases are significan cases for the need of organizational collaboration and information sharing. The two women and their research highlighted many aspects of clinical research that could prevent or help people in their suffering worldwide.

Now we conclude the discussion.

To learn more methods for increased industry efficiency, view our library of resources for clinical research professionals.

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

Clinical research jobs in Pune are increasing and to meet the current requirement of the proficient candidates, you should consider enhancing 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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Interview For Pharma Freshers : Tips & Preparations Part II

Interview For Pharma Freshers : Tips & Preparations Part II

Today we continue with the same topic we were discussing in our previous blog post.

Interview tips

The three aspects of the interview process:

  • Pre-Interview Planning
  • Interviewing
  • Following-up

PRE-INTERVIEW PLANNING

This will make you more confident and keep you motivated. Before you start keep a written or computerized list:

  • Date resume was sent
  • Name of company
  • Name of person you sent it to
  • Address
  • Phone
  • Date and time of interview
  • Results of interview
  • Second interview
  • When you sent a thank you letter or note

You need to find about the company thoroughly, which is very essential but it is often neglected. Try finding out the following information:

  • Products or services
  • Company history
  • Number of employees
  • Business methods
  • Distribution methods
  • Organizational structure
  • Clients or customers -Locations
  • Reputation
  • Philosophy
  • Industry standing/ Sales or activity volume
  • Prospects for company growth

INTERVIEWING

You need to relax and think about all of your skills, accomplishments, and abilities. You should know your strength and weakness. You need to make a resume that would say everything about in details and must be appealing.

Resume

  • Be honest.
  • You need to quantify your achievements with figures and percentages
  • You must think in terms of increasing productivity, decreasing costs, and increasing profit for the company.
  • Try to appear relaxed and alert
  • Be friendly and an enthusiast.
  • Always dress in your formals and be calm in your look.
  • First impressions counts.
  • Groom yourself well.
  • Sit comfortably and with good poise.
  • Ask questions. If you want to clarity certain aspects of the job.
  • Don;’t ask about paid holidays and vacations unless the job is offered
  • Carry extra resumes and references with you.
  • No fancy jewelry please.
  • Be polite.
  • Show a can-do and positive attitude.
  • If asked general questions, answer in terms of your professional abilities and experiences.
  • Never, never criticise former employers.
  • Have good posture and direct eye contact.
  • Give a firm handshake before and after the interview
  • Speak clearly in a firm, confident, and not too loud voice
  • Smile, when appropriate
  • Try to relax
  • Give specific answers to all questions. Don’t be vague.
  • Thanks the interviewer.
  • If you are really keen for the job, tell the interviewer again before you take your leave.

EMPLOYERS INDICATE THAT YOU CAN HURT YOUR CHANCES OF GETTTNG A JOB BY :

  • Poor career plans
  • Under qualified for the position
  • Communication not proper
  • Unsatisfactory evidences of achievement
  • Fail to research the company
  • Displaying a lack of interest in the organization
  • Unwillingness to relocate
  • Appearing more interested in money and benefits than anything else
  • Fail to follow-up post interview

THE GOLDEN RULE OF INTERVIEWING:

Be yourself, know yourself, and sell yourself.

Employers are looking for someone who can contribute to the buisiness by:

  1. Making Money
  2. Saving Money
  3. Saving Time

So keep it in mind.

WE conclude the discussion now. You have to prepare by your own and crack your interview confidently.The above tips are very essential to keep in mind. Good luck!

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 help and guide you in making 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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21 Trends for Nurse Practitioners in 2016 Part II

21 Trends for Nurse Practitioners in 2016 Part II

Today we continue with the blog topic we started a few days back and shall discuss some other points that is making nurse practitioners trending in 2016.

Here I’m discussing a few more and the many more shall be covered in our upcoming articles.

Integrated Care

In 2015, great initiatives were taken in integrating primary care and psychiatric care. The common venture of both the Mental Health Parity and Addiction Equity Act and the Affordable Care Act created the perfect blend to help integration. The new payment models reward healthcare providers for improving patient outcomes while making an effort in reducing overall costs and research. This is what integrations can achieve.

Empowered Patients

The thoughts and views of patients are given a better and more priorities. Now patients can make of use the internet to compare hospitals and select the one with the best clinical prospects, safety measures, and competitive costs. Patients are actively making use of this benefit and choose their healthcare facilities and providers wisely. Thus the well informed patient has become an empowered patient.

Wellness & Employee Health

Now more and more insurance payers and large organizations seek to bear health care costs under the Affordable Care Act. Though similar programs existed earlier, they have currently begun to gather considerable traction. Businesses are now offering their employees free gym memberships, free health screenings, massages, mid-day yoga breaks, smoking cessation classes and weight loss resources.

Bundled Payments

In the year 2015, the Centers for Medicare and Medicare Services announced a number of payment reform models in which they proposed to authorise bundled payments for total hip and total knee replacement in 75 different geographic areas across the region.

This proposal came as a shock for a few medical groups because for the first time, the concept of bundled payments would become a requirement and not voluntary. As 2016 progresses, let’s keep a watch on the outcomes and can anticipate more unique payment models yet to be announced.

ICD-10

The US ultimately implemented the International Classification of Diseases, 10th Edition (ICD-10) on October 1, 2015, to become the last modern healthcare system in the world to adopt this more effective coding system. Originally started by the World Health Organization (WHO) in 1992, ICD-10 designed a coding system that classifies diseases and other health issues such that diagnostic information can be easily stored and retrieved.

Greater Accountability

Now an era of accountable care has begun with the already existing healthcare. Hospitals are now accountable for their patient outcomes and there is forming of Accountable Care Organizations. It’s mandatory for hospitals to demonstrate to the public exactly how and how well they are implementing evidence-based practices. They must also submit reports to the federal government, which then becomes open to the public.

With time, CMS is becoming more and stricter regarding the delivery of accountable care. Those organizations that fail to meet CMS’s criteria are subjected to reimbursement reductions. In the coming years, CMS is likely to increase the penalties and holding the hospitals more accountable for delivering high-quality care.

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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A Dilemma For Big Pharma Companies : CNS Drugs

A dilemma for big pharma companies : CNS Drugs

The central nervous system (CNS) is the most complicated area of clinical research. And currently the big pharma companies are keen to invest in this therapeutic area. But the R&D spends have not yet got rewarded with the desired results. R&D in this area is risky and chances of approving the drugs by the regulatory board are very slim. Hence big pharma companies are at the risk of major losses.

The budget of clinical research for developing a CNS drug versus a cardiovascular drug is 30 percent higher and the chances of a CNS drug reaching a great status in the market is about 50 percent lower.

Research and development by big pharma companies in area of diseases like depression, anxiety, schizophrenia, Alzheimer’s, Parkinson’s and stroke have invited the risks of heavy investments but very less guarantee of success.

The big companies concluded that the risks associated with CNS drug development are very high—so are they justified?

Challenges Facing CNS Drug Development

External pressures have created trouble for the pharma industry’s efforts to address CNS disorders like the active “anti-psychiatry” movement made up of organisations, politicians, religious groups and layman who does not believe the importance of psychiatric treatment.

Moreover there are also the internal pressures. For instance only 8.2% of CNS drug candidates become available for clinical use, compared with 15% of other drugs. Phase II and III of clinical trials and also the regulatory approval; all takes much longer for CNS drugs compared to other therapeutic drugs. Some CNS drugs might take 18 long years from preclinical work to marketing, and clinical research organizations rarely take the benefits of available regulatory tools like Priority Review and Fast Track designation.

Phase III failures

As per reports, most CNS R&D losses of recent years are due to the fact that the majority (4 out of 5) of CNS leads fail the most crucial and expensive phase III stage of clinical trials. And reasons are numerous that includes strict board regulations for CNS disorders to insufficient understanding of the facts underlying brain disease.

What Clinical Research Organizations (CROs) Can Do?

To mention, the figures say that CNS disorder – patients outnumber that cardiovascular disorders ones and with increase in population, the numbers with CNS disorders are increasing. To address this need, there are some ways to enhance the speed of CNS drug development like; implementing proof-of-concept studies, orchestrating studies with a singular drug development team rather than by handing off studies phase by phase, and embracing open, dose-ranging trials followed by moves to a small sample, randomized clinical trial before the move to Phase III. The idea to co-develop CNS drugs with publically sponsored research institutions can also lessen the known risks involved in the development process of CNS drug.

Effective CNS drugs can lessen patient suffering, prolong longevity, improve life-quality and address public health concerns—so it’s essential for all of involved in the drug development process of CNS to look for innovative approaches in bringing these drugs from lab to the market.

We conclude here.

The fact is that disorder associated with central nervous system need to be seriously considered and effective measures in their development process should be initiated.

Amidst many organizations providing clinical research training, 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 CRB’s 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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