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 topic. They can include too much information, making them difficult to follow or too little detail causing them to be ambiguous. Such SOPs can lead to audit observations that the SOPs had not been followed or did not reflect current or acceptable practices.
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
Interpret and Understand your Cannabis Certificate of Analysis (C of A) – All Cannabis Products
July 16, 2021 | 2:00 PM-4:00 PM
Health Canada’s Cannabis Regulations mandates that licensed holders must not sell or export a cannabis product unless testing requirements are met for each lot or batch. Before cannabis product can be made
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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