Live Webinar Data Integrity Key-Considerations | | July 27, 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.
| | July 23, 2021 | 1:00 PM-3:00 PM
Effective SOPs lead a company not only to consistency, quality and compliance but also to executing efficient business operations. Often SOPs are written without consultation with the end user or by someone who has good writing skills but little experience of the
| | July 28, 2021 | 11:00 AM-1:00 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 understanding of the essential elements and
| | Introduction to Pharmaceutical Auditing Techniques | July 19, 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 | | Pharmacovigilance Regulations and Good Pharmacovigilance Practices | August 5, 2021 | 9:00 am – 5:00 pm Live interactive and instructor led
Drug Safety has significantly evolved in the last 2 decades. Regulatory Authorities including Health Canada have focused on Good Pharmacovigilance Practices (GVP) pertaining to the Pharmaceutical Industry.
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