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  • BIOSIMILARS AND ITS REGULATORY CONSIDERATIONS

    About Author:
    Mahendra N. Suthar
    M.S.Pharm. Biotechnology,
    National Institute of Pharmaceutical Education and Research,
    Mohali, Punjab-160062.
    mahendramevada8@gmail.com

  • Opportunity to get Training for Medico-Medical Writing in Tulip Medcom

    Medical writing is part and parcel of drug development process. Medicomarketing communication or healthcare communication has evolved as a profession over a decade. More and more pharmaceutical industries are outsourcing their work to medicomarketing communication or healthcare communication companies/freelance medical writers.

  • KGRL College of Pharmacy invites Professors, Associate Professors, Assistant Professors

    KGRL College of Pharmacy; The Pharmcy profession comprising the Industrial and practice sectors is undergoing a rapid change. Indian Pharma Industry which has registered a spectacular progress today ranks 4th in volume and 13th value in the global pharmaceutical market with exports worth US dollars 2.6 billion besides domestic sales amounting to over US dollars 4 million.

  • Opening for B.Pharm/M.Pharm in Production, DRA, QC at Saudi Pharmaceutical | Require Formulator, Regulatory Affair Officer, QC Chemist

    Saudi Pharmaceutical Industries first and only of its kind manufacturing veterinary and human drugs in Saudi Arabia.
    Saudi Pharmaceutical Industries now manufactures high quality veterinary products and its eminence is compared with European standards. During this short period of time we have not only fulfilled the requirements of Saudi Arabia but also expanded our business to all GCC and number of African countries.

  • Opening in Indian Drugs & Pharmaceuticals Limited - Govt. of India | Require Dy Manager QC, Sr Executive(Regulatory Affairs), Production Supervisor, Sr Chemist (Form. Development)

    Indian Drugs & Pharmaceuticals Limited (I.D.P.L.) is a Central Public Sector Undertaking wholly owned by the Govt. of India engaged in manufacture of pharmaceuticals. A Unit of I.D.P.L. situated at Rishikesh requires to engage trained and experienced professionals in following fields on a fixed term contract basis initially for a period of on e year which can be extended further on performance basis.

  • Working opportunity as QA/RA MANAGER in OREX PHARMA

    OREX PHARMA, one of the leading manufacturers and exporters of the active pharmaceutical ingredients and intermediates. Our head office at thane and plant at dombivli. We are ISO / GMP certified company and we will get our who approval by april end. We are in process of expansion and launching new products

    Post: QA/RA MANAGER

  • Work as Regulatory Specialist I / II OTC GRA CMC 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.

  • Require M.Pharm for Senior Executive/Manager-Regulatory Affairs - 2 posts

    Formula HR consulting, Reputed pharmaceutical company

    Post: Senior Executive/Manager-Regulatory Affairs- 2 No.'s

  • Opening for M.Pharm as Manager - Regulatory Affairs @ VINS Bioproducts

    VINS Bioproducts Limited entered the arena of biologicals and bio-pharmaceuticals at the turn of the century with a view to produce life saving drugs for rural areas. Early on, the company focused on finding remedies for diseases that are endemic in India, the tropics and other less developed nations.

  • Work as Medical Writer in PPD Pharmaceuticals

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