Tuesday, December 24, 2019

Fundamentals of Formulation and Manufacturing

Workshops
Fundamentals of Formulation and Manufacturing



January 31, 2020 | 9:00 AM- 5:00 PM

Pharmaceutical drug products come in a variety of dosage forms and comprise of distinct formulations manufactured according to specific processing instructions. Formulation scientists develop pharmaceutical products in conjunction with specialists in other disciplines such as pharmacokinetics, pharmacology, toxicologists, clinicians and others to ensure the final product is safe, effective and of the highest quality.


Review of the Safe Food for Canadians Regulations and Developing Preventative Control Plans for Domestic Businesses, Importers and Exporters

February 24, 2020 | 9:00 AM-5:00 PM


The Safe Food for Canadians Regulations (SFCR) came into force on January 15, 2019. This 1 day training will provide in-depth guidance to the food industry on the regulatory changes introduced by the SFCR. At the end of the


GMP Fundamentals

January 17, 2020 | 9:00 AM-5:00 PM

Course Outline
  • Definition and History of GMPs
  • GMP & Drug Establishment Licencing
  • The importance and requirements for adequate premises and equipment
  • Personnel hygiene, training and responsibilities
  • Quality Assurance versus Quality Control

Live Webinars
How to Write Effective Standard Operating Procedures (SOPs)

January 23, 2020 | 1:00-3:00 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 topic

Cannabis Micro Licence Application Process and Requirements


January 22, 2020 | 2:00-3:30 PM

The Cannabis Act establishes that an application for one of the Micro Cultivation/Processing Licence must be filed with Health Canada in the form and manner specified by the Minister and must include the information required by the Minister.


Optimization of a Pharmaceutical Granulation Process using Quality by Design (QbD)

March 27, 2020 | 2:00 p.m – 3:30 p.m

For many years pharmaceutical companies have placed considerable effort in developing robust manufacturing processes to assure the highest quality products, minimize defects, eliminate rejects and conform to all Regulatory requirements

Consulting and Training Services
Most importantly, AAPS custom tailors the consulting solutions to
fit your needs. We work side-by-side with you to create solutions that help you achieve what you want to achieve.
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