Pharmaceutical

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New answer posted

9 months ago

0 Follower 9 Views

K
Kanishk Shukla

Contributor-Level 10

Yes, MD Pathology graduates have a growing role in the pharmaceutical industry. They are employed in drug safety, clinical trials, and research & development departments. Their expertise is vital for evaluating the effects of drugs on tissues and organs.

Pharma companies also hire them for quality control, regulatory documentation, and pathology-related decision-making in pre-clinical and post-marketing studies, offering a dynamic and well-compensated alternative to traditional hospital roles.

New answer posted

9 months ago

0 Follower 5 Views

V
Vidhi Jain

Contributor-Level 10

The time required for the BTech Pharmaceutical Engineering course entrance test preparation depends on the individual preparing for the course. You should start with your preparation as early as possible, at least 6 to 8 months before the final exam is scheduled to take place.
This gives you enough time to prepare, cover the maximum portion of the syllabus, and do a thorough revision as well, which increases your chances of getting shortlisted.

New answer posted

9 months ago

0 Follower 8 Views

A
Amisha

Beginner-Level 1

M.Pharm in Manipal Pharmaceutical Institute, Karnataka is very costly. And the placement is also not so high. The average placement is about 40 percent.

New answer posted

9 months ago

0 Follower

M
Mani Sahni

Contributor-Level 10

Yes, MD doctors can work in clinical research, medical affairs, or pharmacovigilance roles in pharmaceutical companies and research organizations.
They contribute to clinical trials, drug development, safety monitoring, and scientific writing. Organizations like ICMR, WHO, and global pharma giants like Pfizer or Novartis actively hire MDs for medically-driven research roles and advisory positions.

New answer posted

9 months ago

0 Follower 4 Views

L
Loveleen Choudhury

Contributor-Level 10

Ethical considerations in Pharmacovigilance ensure patient safety, transparency, and responsible reporting of adverse drug reactions. Professionals must maintain integrity and adhere to regulatory guidelines.

  • Patient Confidentiality – Protecting personal health information in safety reports.

  • Accurate Reporting – Avoiding data manipulation or suppression of adverse drug reactions.

  • Conflict of Interest – Ensuring unbiased reporting free from pharmaceutical company influence.

  • Informed Consent – Respecting patients' rights in clinical trials and post-marketing surveillance.

  • Public Safety Prioritization – Balancing business interests w

...more

New answer posted

9 months ago

0 Follower 4 Views

A
Aishwarya Rai

Contributor-Level 10

Pharmacovigilance professionals deal with various challenges related to data management, regulatory compliance, and evolving safety concerns. Overcoming these challenges requires adaptability and continuous learning.

  • High Volume of Data – Managing large amounts of adverse event reports efficiently.

  • Regulatory Complexity – Adhering to changing international drug safety regulations.

  • Strict Deadlines – Meeting reporting timelines for regulatory compliance.

  • Cross-functional Communication – Coordinating with clinical teams, regulators, and pharmaceutical firms.

  • Technological Adaptation – Keeping up with new safety monitoring tools and

...more

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