All Quality Assurance Consultant Programs Offered by ICS Inc


GMP/cGMP, GLP, GCP, GPP, GVP, ISO 10725, ISO 13485, ISO 13488, Medical Device QMS, ISO 9000, ISO 14000, HACCP/ISO 22000  – Implementation, Training, Auditing, & Validation Studies

Based in British Columbia, but covering all of Western Canada

GMP Quality Assurance ConsultantGMP / cGMP: Good Manufacturing Practices

GMP is an overriding set of principals which govern the quality of every aspect of making a drug. It is a set of regulations, mandated by Health Canada’s Therapeutic Products Program (TPP), that ensures that the product (drug) offered for sale to the public is fit for its intended use and is safe. (Termed cGMP in the USA)


Good Production Practices (GPP):

for the propagation & cultivation of medical marijuana / cannabis



Production facility design & construction oversight servicesFacility Design & Construction Oversight Services to GMP/cGMP Standards

Ensures that your proposed production facilities are designed and constructed in a manner that will comply with the GMP requirements.


GLP Quality Assurance ConsultantGLP: Good Laboratory Practices for Clinical Laboratories

A set of internationally harmonized regulations, mandated by the Environmental Directorate of the Organization for Economic Cooperation and Development (OECD).


Good Clinical Practices (GCP)

for products used in clinical trials, such as drugs, natural health products (NHPs), cannabis & extracts, and medical devices.


images16   GVP:  Good Pharmacovigilance Practices

           for drug Adverse Reaction Reporting (ADR)


HACCP / ISO 22000 Quality Assurance ConsultantHACCP / ISO 22000 for food production

HACCP (Hazard Analysis and Critical Control Point) is a scientific system used in food production, to prevent problems, by applying controls at points in a food production process, where hazards could be controlled, reduced, or eliminated.

iso 9000 Quality Assurance ConsultantISO 9000 for manufacturing & services companies

This is a system to effectively manage your business, in order to provide your product or services to your clients, in a consistent, accountable, and traceable manner.

ISO 13485 / ISO 13488 Quality Assurance ConsultantISO 13485 / 13488 Quality Management System (QMS) for medical devices

This standard is presently regulated by Health Canada’s “Therapeutic Products Programme” (TPP) and is similar to the European Union’s EN 46000 Standard. It is soon to be a requirement in Canada, in order to harmonize with other parts of the world. ISO 13488 is the same as ISO 13485, with the exclusion of the requirements for “Design Control”.

ISO 14000 EMS Quality Assurance ConsultantISO 14000 Environmental Management System

A set of internationally created and recognized guidelines (EMS) that allow companies to address the environmental impact of their products, services and business practices. Its focus is on prevention and continuous improvement.

ISO 17025 Quality Assurance ConsultantISO 17025 for testing & calibration labs

This standard was developed specifically to give guidance to lab managers on both quality management and the technical requirements for the proper operation of a laboratory. Thus, ISO 17025 can be thought of as the technical compliment to ISO 9000. As a matter of fact, any organization who meets the requirements for ISO 17025 automatically is ISO 9000 compliant (but the converse is not true).

Process & Equipment Validation servicesValidation Service

This is the documented act of demonstrating that any of your critical procedures, processes, equipment, materials, activities, or systems will consistently lead to expected results.


Auditing Servicesinternal audit & third party audit services

To assess compliance to the regulations.


Stability Protocol is mandated by Health Canada’s Good Manufacturing Practices (GMP). It is to determine the normal shelf life of the product under recommended storage conditions.

Security Requirements

For Narcotics & Controlled Substances, including for cannabis (marijuana) under the ACMPR-MMPR.

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