ISPE CEUs: 1.3
Type: Classroom Training Course
Due to the growing pressures from global competitors, high marketing demands, and the requirements of GMP compliance, the bio-pharm industry (brand drugs and generic drug companies) are looking beyond the usual group of closely-knit suppliers. India and China engage in bulk activities and have been generating new dimensional API products with more specialized capabilities than those required by traditional drug products. In order to remain competitive, API manufacturers will need to attune themselves to this evolving dynamic global market.
This classroom course covers areas in which compliance requirements differ most from traditional pharmaceuticals and biologics and will review common deficiencies and problem areas related to the ICH Harmonised Tripartite Guideline Good Manufacturing Practice Guide For Active Pharmaceutical Ingredients Q7 and the USFDA's interpretation of ICH Q7, as defined in Q7A, the Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients.
The course also discusses the manufacturing equipment system and engineering practice and compliance issues. Participants will learn key regulatory information and practical utilization techniques to develop the ability to ask the right questions based upon science and the regulations knowing the relationship between this quality guidance for the production of APIs, and GMP regulations applicable to the production of pharmaceutical and biologic finished drug products.
Note: We recommend participants have a basic understanding of the GMP regulations and API manufacturing operations.
Professionals in quality assurance, quality control, DS (drug substance) development and manufacturing, plant management and production managers/supervisors, maintenance/utility engineers for facility/utility systems and production systems. Design engineers for manufacturing equipment and control systems, design/installation/CQV and regulatory inspectors related to the production of API.
This training course is of particular interest to existing and future members of the ISPE Active Pharmaceutical Ingredients Community of Practice (COP).
|Daily Schedule at a Glance|
|07:00 – 08:30||Registration Open|
|08:30 – 17:00||Training Course|
|10:30 – 11:00||Refreshment Break|
|12:00 – 13:00||Lunch|
|15:00 – 15:30||Refreshment Break|
BY 14 Jan
AFTER 14 Jan
Group discount applies to Member/Nonmember rate only. To qualify, all registrant information must be submitted at the same time. Registrations that arrive later will NOT be eligible for the group discount. Cannot be combined with other offers. To register as a group, please contact ISPE by telephone, +1-813-960-2105 or by email, email@example.com.