Auditor – Good Manufacturing Practices (GMP)
This training addresses the auditing of pharmaceutical product supply chains, from the producers of raw materials, to the manufacturing of bulk product and follows the requirements of ICH Q7A Good Manufacturing Guidance for Active Pharmaceutical Ingredients (API).
The regulations for GMP compliant manufacturing of drug products are laid down in the laws and directives of the USA, EU, Canada and Japan. Part of this GMP guidance is the mandatory training of all personnel (including technical, maintenance, and cleaning personnel and all others whose activities could affect the quality of the product) that perform duties (for example, manufacturing, processing, packing, or storage of drug products) in production areas and control laboratories.
Continuous basic training on the theory and practice of GMP should be given to all employees and contractors.
On training completion you will be able to:
Understand GMP requirements for ac
- Asking Price : 25000
- Tuition Type : Others
- Author First Name : Tania
- Author Last Name : Saini
- Author Email : firstname.lastname@example.org