Tag Archives: clinical research vacancy

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.
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.
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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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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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How To become A Clinical Research Scientist?

How To become A Clinical Research Scientist?

Clinical Research Review presents the road map to become a clinical research scientist. This would help those who wants to make a career in clinical research.

Clinical research scientists does medical research for the welfare of health in humans and/or animals. Clinical research trials are one of their methods of investigation. Here is a chart giving an overview of how to enter this sector:

Degree MD &/or PhD degree
Field of Study MD: medicine
PhD: biology
Responsibilities Laboratory research & analysis for medical innovations; publication of research

Basic Education For A Clinical Research Scientist

There are various educational paths to become a clinical research scientist. Many clinical researchers have medical degrees, doctorates in a natural science or both. One can begin the pursuit of this career with a regular bachelor’s degree. A course of study in or related to the field of life science is highly recommended. The coursework in this area should include general biology, mathematics, physics and more specialized topics such as cell biology. Medical and doctoral programs are highly selective, so a strong academic record is desirable.

An Advanced Degree Program in Science or Medicine

Most clinical research scientist positions require either an advanced degree in the biological sciences or a medical degree. Graduate degree programs in cellular and molecular biology, neuroscience, biochemistry or microbiology often satisfy this need. Some universities offer master’s degree programs in clinical research. Alternatively, obtaining a Medical Doctor (M.D.) or nursing degree may qualify individuals to work in the field.

The success tips is that consider attaining a dual degree. Many clinical research scientists choose to complete a dual degree program with majors in science and medicine. In fact, some job postings require that candidates possess dual degrees. Students in these dual degree programs learn about medical practices and advanced research methodologies. Possessing two graduate degrees may make students eligible for more job positions after graduation.

Work as a Clinical Research Associate

The clinical research scientists typically begin their careers in fresher positions, possibly as a clinical research associate. These associates assist research scientists in designing and carrying clinical trials. They also help validate gathered data and monitor the procedures to assure that the process complies with professional protocol. The success tip is earn a certificate like the Certified Clinical Research Associate, Certified Clinical Research Coordinator and Physician Investigator. Earning any of these certifications requires clearing an exam. These certifications are recognized in the industry as indicating various job skills and, may help individuals advance in their careers.

Work as a Clinical Research Scientist

Clinical research scientists can work at universities, pharma companies, clinical research organizations, hospitals or for the government. These scientists perform analysis on cells, tissue and organs to identify microbes and toxins with the goal of understanding the reason of diseases and being able to develop vaccines or medicines for treatment. Some clinical research scientists may work directly with patients in health care centers by administering clinical trial drugs and therapies.

Research scientists have chances to advance to supervisory or lead positions with enough experience and strong performance.

The Success tip is to Participate in continuing education. Knowledge in scientific fields changes rapidly. Clinical research scientists may find it advantageous to participate in continuing education courses offered by professional organization. Such professional training may come in the form of conferences, webinars, online classes or in-person courses.

In the race of many institutes CRB Tech Solutions has it own name in offering Clinical Training.

Clinical Research review by CRB Solutions is enough to make you consider and take up a 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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Apple Plans Transform HealthKit From Tracker To Diagnosis Tool

Apple Plans Transform HealthKit From Tracker to Diagnosis Tool

Till date Apple’s HealthKit has mostly collected fitness data from its devices. In the future, if the company finds its way, the software will interpret that information, converting it into advice for users, doctors and others.

Many health care experts hired by Apple in recent years are designing enhanced electronic health record software that can well analyze and understand the implications of patient data.

The iPhone manufacturer is even working on new apps for the Apple Watch. It can track users’ sleep patterns. Another app focusses on fitness levels by calculating the time taken for the heart rate to fall from its peak to resting level. Apple already has an app that measures heart rate, but yet don’t interpret them.

The ultimate goal of Apple’s health care technology team is to turn HealthKit into a tool that improves diagnoses. The system could do away two problems that plague the field of clinical research and have stumped other specialist firms in the field.

Chief Executive Officer Tim Cook wants Apple to act more in improving software and services to secure new sources of economy and make customers more dependent on the company’s devices.

In early this year, Apple bought Gliimpse Inc., a startup that build software to pull electronic health records from different databases and in different formats and finally store them in one place.

He equated the product to Apple’s music business. That negan with the iPod, but as more people became habituated to storing all their music files digitally, Apple united all music lovers in a single platform on top of the device.

Apple health software might become a revenue driver, too, by keeping people intrigued to the company’s equipments. If a patient’s health records, and related suggestions, are reachable through Apple’s system, it would be difficult to trade in an iPhone for a smartphone running Google’s Android OS, and its health-tracking software Google Fit.

The second module of Apple’s Watch has a built-in GPS tracker, faster processor and is water resistant and many people can run, swim and do other exercise with the device. The upgraded Watch software, dubbed watchOS 3, puts health tracking information more prominently in the user interface, and adds a breathing during exercise app as well as tracking during swimming.

Building more sensors into the Watch serves a limited purpose. The accelerometer can generate most of the useful data needed to monitor a person’s well-being. A glucometer or blood-pressure sensor would only help a small percentage of users, the person said.

Scott Jenkins, said that Apple is working hard with many of these large institutions to produce tools that are medically significant, to take data from sensors.

Stephen Friend, a Merck & Co. veteran who founded health data non-profit Sage Bionetworks, is honored with being the brains behind ResearchKit. He joined Apple as full-time employee in June after working as a consultant for more than two years.

Yoky Matsuoka, formerly technology chief at Google’s Nest Labs unit, joined Apple’s health team last year. Nest mostly known as a hardware specialist, but Matsuoka head the development of software that interpreted and learned from data that its internet-connected thermostats collect.

Apple’s greatest obstacle for now is proving to medical professionals that data delivered from wearables through HealthKit and ResearchKit is reliable.

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

Clinical research jobs are increasing and to meet the increasing requirement of the peofecient professionals , 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.

Related Topics:

1) Top 10 Clinical Research Companies in Pune

2) Clinical Research Organization

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Rise In Mercury Brings Down Swine Flu Cases

Rise In Mercury Brings Down Swine Flu Cases With the soaring temperatures, swine flu cases which makes people in majority vulnerable seem to have subsided. Only a few patients are tested positive for the H1N1 virus out of total patients who took admission in hospitals.

Dr Charan Singh, nodal officer for swine flu in the Health department in the capital, said that every year, with a rise in temperatures, the virus tends to recede. Hence there are fewer cases now. Cases would have come down more but owing to the unseasonal rains, some cases yet exist.

As per reports of 2015, since January 1st , 4,266 patients tested positive for the virus in Delhi with 1,500 being reported in the month of March. There are reports of twelve deaths from the capital, including two pregnant women and one child.

Health officials told that required arrangements for swine flu, including treatment and diagnostic facilities, will be kept functional till the cases subside completely. Isolation wards remain closed from April-May, but that time it was kept open. An official reported that doctors are expected to continue with treatment guidelines of category A, B and C patients. The nodal officer said that in most of the cases, patients have been suffering from conditions mainly diabetes, heart and respiratory diseases.

As reports of an official from the Union Health Ministry, the year 2015 also saw majority number of deaths and huge number of cases as per reports in the last 6-7 years. It claimed the lives of approximately 2,200 people and affected another 35,000. While 981 deaths were reported along with 27,236 cases of swine flu in 2009, the disease claimed the lives of 1,763 people in 2010 and affected around 21,000 people. In 2011, 603 cases were reported and swine flu claimed 75 lives while, in 2012 there were 5,045 cases and 405 deaths. Swine flu claimed 699 lives and affected 5,254 people in 2013. In 2014, 938 cases were reported and 218 deaths were caused by the virus.

With advise to the people, Singh said them not to “panic”. He continued ro state that H1N1 is a self-limiting disease and if treated in the early stages, chances of complications are quite less. There are no reasons to panic as most of the cases reported are of seasonal common cold or flu. He added that people should simply maintain routine hygiene. The Health department authorised the private hospitals with more than 50 beds and equipped with ventilators to treat swine flu patients. The new guidelines have included 122 private hospitals to treat H1N1 patients, along with 19 government and seven private ones that was previously designated as authorized centers.

The fact is that as soaring temperature reduce swine flu incidence; rains increase it. The unseasonal spell of rain has come as a dampener for the district officials of health department who were hoping that cases of swine flu would lessen with a rise in temperature. The rains have caused drop in temperature making it favorable for the virus to spread.

Well its clear that the only way the incidence of swine flu remains suppressed is higher temperatures and rains can worsen the conditions.

In the race of many institutes CRB Tech Solutions has developed a niche. Its very popular in offering the best training in Clinical Research. This clinical research institute has created a place for itself in this field.

Clinical research jobs are increasing rapidly and to meet the increasing need of efficient people , you should consider upgrading with clinical courses.

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

Related Posts:

1) Stem Cells Therapy- A Hope For  Parkinson’s Cure

2) Clinical Research for Pulsing in Veins

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Pharmacovigilance In Product Lifecycle

Pharmacovigilance In Product Lifecycle 

Part 1

Risk Management Planning critical for patient safety and product innovation

A safety signal is a possible relation between an adverse event and a drug, or a new aspect of a known adverse event and a drug, which involves some type of further investigation.

When a signal is detected, further investigation is needed to determine whether an actual relationship exists. The whole process of signal management is one of the most crucial steps in PV and is explained in numerous guidelines to various degrees. These includes the EMA Guideline on Good Pharmacovigilance Practices (GPV) Module IX.

Now signal management includes many processes, such as identifying sources of data, detection of signal, setting of priorities, analysis, evaluation and assessment with recommendations for action, and remains at the center of PV and drug safety. These processes are required for patient safety and by drug regulatory agencies. Keeping of records and documentation of the decisions, activities and results is also required. The outcome of the signal management process is dependent on the quality of the safety data and, as a result, improvements in the quality of safety data will have an impact on the effectiveness of signal management and PV as a whole.

The area of safety signal detection has come into focus over the past years and is growing in importance. It is well accepted that statistical methods of signal detection can initiate certain drug-event combinations for in-depth analysis from a medical perspective, potentially leading to confirmation of proof and signal identification. Signal detection can be completed using many methods, each of which has some advantages and limitations. New and improved computer-aided statistical methodologies are under assessment with the anticipation of offering improved specificity, sensitivity and predictive value.

The revised guidelines says about the importance for medicine developers to engage in early dialogue with EMA and other stakeholders, to achieve an understanding of the data package to be included in the application, including on the proposed risk management plan. Such risk management planning is critically important in particular in the context of conditional marketing authorizations.

During the yearly renewal of such authorizations an evaluation of the data accrued during the post -authorisation period takes place. The evaluation considers whether an update of the product information or risk mana gement plan is necessary.

Companies encouraged to seek scientific ad-vice for PASS

What’s new?

In the year, 2015 EMA started a pilot to encourage businesses to seek scientific advice for post-authorisation safety studies . This voluntary procedure will help to upgrade the planning for and the mode of studies meant to collect further info on a medicine being safe once it is on the market.

What do you need to know?

Any question relating to the collection of data and information on a medicinal product, or on risk minimization can be submitted via the scientific advice procedure. EMA encourages companies to get scientific advice in particular on non -imposed PASS.

What’s new?

In September 2015, EMA initiated the Patient Registries Initiative to make good use of existing registries and help the establishment of high-quality new registries.

The data collection from a patient registry is often needed of a marketing authorization holder (MAH) as part of a package of benefit-risk management measures on the safety or efficiency of individual products in routine clinical practice. Despite the previous existence of a disease registry, MAHs sometimes seek to establish their own product registry, potentially resulting in duplication of ef forts and a slow resolution of the starting concern. The initiative proposes a strategy to identify and evaluate current data sources and develop a methodological toolkit for establishing new registries if required. The initiative begins with a pilot phase to test different components of the patient registry process and if it meets regulators and other data and information requirements.

If you are seeking for Clinical research courses in Pune, then CRB Tech Solutions has created a niche for itself. Its known for offering the best of all training in Clinical Research.

Clinical research jobs are rapidly gaining significance and to meet the need of good professionals , you should consider improving yourself with clinical research institute .

This Clinical Research review of CRB Tech Solutions will help you support your clinical research career .

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TOP 5 Clinical Research Organizations(CROs) In India

Introduction:

The clinical research industry is continuously undergoing a positive development in India. Gradually, the clinical researches are being viewed as drug discovery rather than drug development destination only. At present, many companies are looking for innovations. The famous players that are operating in the nation include MNC CROs which are dominating the country’s market . And, it is becoming important for each and every one of us to know about the popular CROs that are functioning in the nation.

This article would give an idea about some of the famous Clinical Research Organisations in the country.

The CROs that are operating in the country can be divided into two major categories:

  • Global Players with their presence in India
  • Domestic Players

Famous Global Players:

Following are a few of the famous global CROs who are having their presence in India:

Quintiles: Founded during the year 1982 when Dennis Gillings, a London based professor signed his first consulting contract. This company began its global expansion during the year 1987 and in the year 1993, the company made its entry into Asia.

Currently, this company covers the Asian continent by opening its services in around 20 cities including Bangalore, India. In our country, Quintiles has five offices in the below locations:

- Ahmedabad

-Bangalore

- Mumbai

- New Delhi

Quintiles India has the pride of holding some of the best relationships with the leading medical centers as well as with some of the experienced principal investigators.

The key services of Quintiles in India are Project Management, Clinical Trial Monitoring, Site Management, Drug Safety, Regulatory Affairs,Quality Assurance and Pharmacovigilance.

PPD: It is one among the leading clinical research organizations which was founded in the year 1985. This company has its offices in as many as 50 countries with a total number of 84 offices. In India, the company is functioning in the following three locations:

- Gurgaon

- Bangalore

- Mumbai

The clients and partners of PPD include pharma companies, medical device manufacturers, Biotech companies, academic institutions and government organizations.

And, the services that are oferred by PPD are clinical development services,laboratory services, – Consulting Services and making innovation

Paraxel: A premier provider of clinical trial services to the biopharma companies as well as the medical equipment businesses for the development of novel medical therapies across the globe for more than 30 years. Paraxel is operating in India, in the following locations:

- Delhi

-Hyderabad

- Bangalore

- Gurgaon

- Mumbai

- Chandigarh

Paraxel is offering the following services:

- Early phase services

- Phase II-III services

- Peri-approval services

- Post-approval services

- Clinical logistics services

- Consulting services

Famous Domestic Players:

Siro Clinpharm: Founded in the year 1996 by Dr. Gautam Daftary. The company started operating in Mumbai.This company also has its offices in USA and Malaysia. Various services that are being offered by this Indian CRO are:

- Clinical operations

- Clinical data management

- Medical writing

- Scientific writing

-Biostatistics as well as Statistical programming

- Clinical trial supplies

The therapeutic expertise of Siro Clinpharm includes:

- Oncology

- Cardiovascular Disease

- Central Nervous System

- Endocrinology

- Respiratory Diseases

- Infectious Diseases

GVK Bio: This is one among the Asia‘s leading discovery research and development organizations. This company has its global customer base of over 300 satisfied customers. The headquarter is located in Hyderabad. In India, the company is operating in the following locations:

- Hyderabad

- Bangalore

- Mumbai

- Gurgaon

- Ahmedabad

The services that are being offered by this CRO are:

- Discovery services

- Clinical development services

- Formulation R&D

- Manufacturing services

- Information & Analytics

- Integrated programs

Clininvent: Clinivent is the company which was established as the Contract Research Organization that is having great capabilities in the areas of clinical trial and data management. The company is located in Mumbai. The partners of this company are:

- TCG Lifesciences

- LabVantage

- Chembiotek

Various services that are being offered by this Clininvent are as follows:

- Clinical trial management

- Data management

- Pharmacovigilance

- Medical writing

- Quality assurance

- GCP training

CliniRX: CliniRX Tangent Research has been developed as an affiliate of the JK Organization which is a 125-year old entity. The JK Organization has its headquarters in India. Various services that are being offered by CliniRX are as follows:

- Site selection

- Project management

- Monitoring

- Site support

- Medical writing

- Safety surveillance

- Clinical compliance

- Biometrics

The research offices of CliniRX are located in:

- Bulgaria

- Netherlands

- United States

- Israel

In the competition of many organizations in Pune CRB Tech Solutions created a big name. Its very popular in offering the best training in Clinical Research.

Clinical research jobs demands are increasing and to meet the increasing need of excellent professionals , you should excel yourself with our clinical research institute.

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

Related Topic:

1)Clinical Research and Scandals

2)Clinical Trials : In The Clouds

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The Suboxone Challenge

People who works in pain or addiction research might be familiar with a Naloxone Challenge, when a patient is administered the opioid antagonist drug naloxone to determine if they are opioid dependent, but in this blog we introduce you to the social issue facing many addicts, which is termed as the Suboxone Challenge.

In the Journal of Clinical Pharmacology there is an article by Dr. Lorraine Rusch of Vince & Associates Clinical Research which explains a widespread issue facing the US today – the opioid addiction

According to the reports of the Institute of Addiction Medicine,though the population of the US is lesser than 5% of the global population, 80% of the opioids and 90% of the hydrocodone used worldwide is used by Americans. AS per estimates of Centers for Disease Control and Prevention, 2.2 million Americans abuse opioids and 1.8 million are dependent on them, thus they are not able to stop taking them without going into withdrawal. That’s approximately 4 million people in the US who are either abusing or addicted to prescription opioids. To put that in perspective for you, it’s the population of Oregon.

So, how do these people could get help for their addiction? Presently, treatment options in the US are extremely limited for substance abusers. There is an exceptionally good article in The Huffington Post, “Dying to be Free,” about the challenges abusers face when looking into treatment choice.

Historically, there has been a lot of resistance to the usage of Suboxone (a drug made with buprenorphine hydrochloride which helps in reducing the symptoms of opioid dependence), which many in the medical world see as the best treatment available. The thought process behind the resistance to Suboxone is numerous physicians and addiction counselors along with many members of the legal system believe that abstinence is the preferred treatment as with alcohol addiction. The author of “Dying to be Free” discusses the insufficiency of the 12-step program used for alcoholics when translated for opiate addicts. But why? When a person abuses opioids for extended periods of time their brain function is altered. Their brain changes literally.

So, what is the state of Suboxone? Why is it so difficult to get this treatment to the patients who requires it? While the National Institute on Drug Abuse has tried to increase the use of Suboxone and Methadone, many places have pushed back by limiting the number of physicians allowed to prescribe these drugs and limit the amount of times they can prescribe it in a year. Because of excessive regulation and the fear of non-compliance, it’s not surprising there is a shortage of doctors in addiction medicine.

So where does the future see? It’s really in the hands of government agencies like NIDA and the US Department of Health and Human Services who are committed to understanding addiction and working with the biopharma companies to fight this problem. Vince & Associates Clinical Trials conducts multiple Human Abuse Liability and Abuse Deterrent Formulation clinical researches each year and stands with the government and innovative companies to develop new medications that can help in reducing the rates of opioid addiction and abuse while still providing pain relief to those who need it.

There are only a few clinical trial organizations in Pune, and CRB Tech Solutions has created it’s own niche. Its known to gives the best Clinical Research training.

Clinical research jobs are increasing fast in Pune and to meet the emerging need of good professionals , you should consider increasing your efficiency with clinical courses.

The Clinical Research review by CRB Tech Solutions will guide you in obtaining your clinical research career.

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