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  • Opportunity for M.Pharm, M.Sc to work as Manager - ANDA @ Biocon

  • HBL invites Deputy Manager - Formulation, Production, QA, QC, Regulatory Affairs, Animal House

    HLL Biotech Limited (HBL) is a 100% subsidiary of HLL Lifecare Limited, a Mini Ratna Schedule B Central Public Sector Enterprise under the Ministry of Health & Family Welfare. HBL is setting up a vaccine complex at Chengalpett, Chennai for manufacturing of Bacterial and Viral Vaccines & developing a strong R&D base for vaccine technologies within the country.

  • Work as Regulatory Affairs Specialist in PPD Pharmaceuticals

  • News

    Daily Updated Pharma-News regarding R&D, FDA, F&D, Pharmaceuticals industries, Hospital Pharmacy and Pharmaceutical Development ...

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  • Career for Global Regulatory Affairs GL Regulatory Specialist I/II in Novartis

    A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people.

  • Career for Drug Regulatory Affairs Business Franchise/Regulatory Coordinator (RC) in Novartis

    A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

  • INVOLVEMENT OF HEALTHCARE REGULATORY AFFAIR PROFESSIONAL IN OVERSEAS REGISTRATION PROCESS

    About Authors:
    ANUJ SINGH
    VINAYAKA MISSION’S UNIVERSITY
    Salem – 636308, Tamil Nadu
    anuj.dra@gmail.com

    ABSTRACT:-
    Healthcare Regulatory Affair Professional with their experience and strong motivation to excel in the Regulatory field has an ability to motivate & give support and strengthen to teams members, involved in process of product registration. Professional has taught a self-starter with the proven ability to prioritize and manage projects in a busy, fast-paced, multitasking environment, along with their experience in establishing relationship with the decision makers & coordinator. The Pharmaceutical industries are among the most highly regulated industries in the country. As India is growing very rapidly in pharmaceutical sector, there is a need of regulatory affairs professionals to cater the current needs of industries for the global competition. Regulatory affairs professionals are the link between pharmaceutical industries and worldwide regulatory agencies. They are required to be well versed in the laws, regulations, guidelines and guidance of the regulatory agencies. There is a growing need to incorporate the current requirements of pharmaceutical industries in the standard curriculum of pharmacy colleges to prepare the students with the latest developments to serve the industries. The present article discusses the regulatory education and its need, learning resources, courses available, syllabus contents and job opportunities in regulatory affairs.

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  • Require DRA Executive in Marion Biotech - 2 posts

    Marion Biotech strongly believes in an integrated approach to healthcare. It is also engaged in extensive Research & Development of unique Herbal products. At Marion Biotech, we set Stringent Standards of Quality, Safety and Efficacy for all the Products that we manufacture.

  • Torrents Pharmaceuticals invites for Regulatory Affair Executive - 3 posts

    Torrent Pharmaceuticals Limited, is a dominant player in the therapeutic areas of cardiovascular (CV) and central nervous system (CNS) and has achieved significant presence in gastro-intestinal, diabetology, anti-infective and pain management segments.

  • Career as QA ,DRA Executives/Managers in Batavia Exports International

    A service oriented export trade company specialized into overseas distribution and manufacturing of pharmaceutical formulations, active pharmaceutical ingredients and related chemicals. Right since the inception of this company since 1985 we are involved in the same activity.
    We associate with several manufacturing units and manufactuing is done in compliance with GMP norms.

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