Raw material requirements in a cGMP environment are often overlooked as a company develops new products. Depending on the product being developed, e.g., tablets and capsules vs. biotechnology products, as few as fifteen to twenty or as many as sixty raw materials need to be sourced before the process can be moved from initiation through completion.
This highly interactive two day seminar on raw material requirements in a cGMP environment will:
Note: Use coupon code 232082 and get 10% off on registration.
For Registration - http://www.complianceonline.com/raw-material-requirements-health-canada-usp-ep-in-a-cgmp-environment-issues-and-solutions-seminar-training-80218SEM-prdsm?channel=pickevent
Course Description: All facilities manufacturing pharmaceuticals, biologics,...
Q
Course Description: In this two day workshop conference you will learn the...
Q
Course Description: Trade Compliance plays a prominent role in international...
Q
Course Description: This course is designed to introduce to individuals the...
Q
Course Description: Risk Based Internal Auditing (RBIA) is defined by the...
Q
Course Description: FDA inspection and oversight of quality control (QC)...
Q
Aims Recently, a series of headline-grabbing operational risk incidents at...
Q
Course Description: Is your company at risk for non-compliance? Is your...
Q
Course Description: Are the financial transactions within your organization...
Q
Course Description: If an internal audit is to assess the effectiveness of the...
Q
Course Description: The objective of this two day "Essentials of USP...
Q
Global Food Supply Chain Risk ...
Q
Course Description: The growth of the medical software industry outpaces the...
Q
Course Description: This interactive one and a half day course led by Ms. Rita...
Q
Course Description: This seminar will cover auditing human resources practices...
Q
Course Description: Importing products regulated by the FDA has become more...
Q
Course Description: This two day seminar will focus on internal controls...
Q
Course Description: Organizations of all kinds and sizes are increasingly...
Q
Course Description: Formal written Standard Operating Procedures (SOPs) are...
Q
Course Description: If you are looking for the answer to the following...
Q
Course Description: A growing public demand for supplements has resulted in a...
Q
Course Description: Significant changes in the regulations and...
Q
Course Description: Significant changes in the regulations and industry...
Q
Course Description: Supplier selection and management is one of the critical...
Q
Course Description: This 2-day seminar is designed to assist companies that...
Q
Course Description: Naturally, getting a project to deliver on time, within...
Q
Course Description: This interactive two day seminar will cover the various...
Q
Course Description: This seminar will help you understand the regulatory,...
Q
Course Description: Regulatory professionals have to write highly technical...
Q
Course Description: This GRC Professional Seminar will teach you how to...
Q
Course Description: Bribery can often damage your business and your...
Q
Course Description: This two day course will prepare firms for a quick,...
Q
Course Description: Unlike risk management, which involves managing potential...
Q
Login to comment