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Physicians play a crucial role in the successful development
of new diagnostic and therapeutic drug. The leading role of physicians is that
they have high-level responsibility for the evaluation of safety and efficacy of
a new potential drug and also for the safe performance of the clinical studies.
For various research and developments of new drugs, physicians also work for
various clinical research organizations (CROs) and biopharmaceutical companies.
Therefore, they are known as pharmaceutical physicians. The physicians involved
in the drug development process usually advises the safety monitoring of drugs,
registration, and evaluation of the drugs, medical research, pharmaceutical
product development, and marketing of medicines among patients. The inputs of
these pharmaceutical physicians are not only limited to medical aspects but
also covers ethical aspects and business responsibilities as well. The role of
physicians in the drug development and also in the pharmaceutical companies has
undergone a transformational change. Many external changes in the
pharmaceutical industry like safety surveillance and regulatory conditions
shows the importance of doctors in the drug development.
Role of physicians in drug development:
Doctors lead and advise on the development of new
treatments, establishes pharmaceutical products, and areas of unmet medical
need. This includes advising on the medical aspects of:
The physician can also use his/her clinical expertise for
the following functions:
Physicians role in drug safety:
The study of serious adverse events (SAEs) and drug safety is known as pharmacovigilance, and nowadays it is one of the most important topics within the pharmaceutical industries. Therefore the role of drug safety physician is the evaluation of safety information and also the addition of the initiatives of various clinical research physicians handling the research and development plans focused on efficient measurements.
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