September 23, 2021 | 2:00 PM-3:30 PM
Data integrity is a key component in making informed decisions within any regulated organization. Reliable data promotes good decisions. Unmanaged and inaccurate data will have consequences on a company’s quality output, state of compliance, the risk to patient safety, and ultimately, the bottom line. There are many risks inherent in poor data management. Without the ability to eradicate these risks, gaps will inevitably exist and a quality system will not reach a reliability level that government agencies such as the FDA, expect to see.
| | September 22, 2021 | 1:00 PM-3:00 PM
This webinar examines the history, rationale, purpose, and GMP requirements applicable to the manufacturing, packaging and labeling, testing, and control of pharmaceutical products and consequence of inaction. Gain practical knowledge in
| | Sanitation Program for Cannabis Production – Cannabis Act | September 24, 2021 | 2:00 PM-3:30 PM
This course and workshop concentrate on three important aspects of an effective sanitation program; Premise, Equipment
| | Introduction to Pharmaceutical Auditing Techniques | October 1, 2021 | 9:00 am – 5:00 pm Live interactive and instructor led
Auditing of contractors, vendors, and suppliers in the Pharmaceutical industry is not only a regulatory requirement but also a critical Quality practice. Companies are outsourcing more and more of their capabilities to outside experts but the | | Quality Assurance for Cannabis Certificate Program | October 5-8, 2021 | 9:00 am – 5:00 pm Live interactive and instructor led
The quality department within a cannabis company is responsible for activities that have impact on the quality, safety or efficacy of the cannabis. They are also responsible
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