• Seminar on Risk Analysis in Pharmaceuticals at NIPER, Mohali

    • October 16, 2019
    • Posted By : admin
    • 0 Comment

    Seminar on Risk Analysis in Pharmaceuticals

    At: NIPER, Mohali

    On– 1st November 2019

    About the Organizer: National Institute of Pharmaceutical Education and Research, S.A.S. Nagar is an Indian public Pharmacy research university, and a part of the seven schools, under India’s Ministry of Chemicals and Fertilizers. The institute offers Masters and Doctoral degrees in pharmaceutical sciences. The institute offers a 2-year PG degree course; MS (Pharm.) in 13 disciplines ( Medicinal Chemistry, Pharmacology, Toxicology, Pharmaceutical Analysis, Clinical Research, Pharmacy Practice, Natural products, Biotechnology, Pharmacoinformatics, Traditional medicine and Pharmaceutics) and MBA (Pharm.)

    About the Seminar: US-FDA, in 2002 had announced its cGMPs a risk-based and defined RMP as a strategic safety program designed to decrease product risk by using one or more interventions or tools. An RMP program starts with identifying the possible risks (and benefits) associated with a product or with the process used to develop, manufacture and distribute the product. Thus, the risk analysis of a pharmaceutical product includes its manufacturing processes, analytical procedures, various supporting facilities at various stages of product manufacture and supply, distribution channel of the product. With risk management tools, the pharmaceutical industry and regulators can manage and assess risk.

    This seminar shall provide an insight into the need for Risk Analysis, Risk analysis associated with manufacturing processes and analytical procedures. The target audience includes personnel from the industry and academic researchers.

    Topics of Seminar: The following are some of the topics that shall be deliberated in the seminar:

    • Need for Risk Analysis
    • Risk analysis associated with manufacturing processes
    • Risk analysis associated with analytical procedures
    • QbD in manufacturing of dosage formulations
    • Hazard Analysis and critical control points
    • QRM: Principles and Industry case studies

    How to Register?: Interested candidates can register for the seminar by filling the registration form available here.

    Registration Fee

    • Rs 3000/- per delegate
    • Rs 2000/- for SMPIC members
    • Rs 800/- for students

    The fee includes course material in the form of CD, lunch, refreshments, tea/coffee and excludes accommodation charges.

    On-site Registration: The on-site registration desk will be open on the day of the seminar from 9.00 am to 9.30 am. An additional fee of Rs. 500/- will be charged for on-site registration.

    Registration Deadline: Oct 28, 2019

    Contact: Phone: 0172-2292032,

    Email: smpic[at]niper.ac.in

    Official Notification


You Might Also Like

No comments found



error: Content is protected !!