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WHY CHOOSE AAPS
AAPS Consulting consists of multiple subject matter experts and has a proven track record of successfully helping companies submit Health Canada and other global regulatory documents, obtain licenses, and maintain compliance. We are committed to prioritizing your needs and delivering the desired outcome.
OUR CLIENTS
OUR CONSULTING SERVICES
AAPS is your partner for consulting and training services. Our commitment to providing quality solutions has led AAPS to be recognized as a strong partner for a number of global pharma.
We have access to and work with some of the brightest minds in Quality, Compliance, Laboratory, Safety, Regulatory, R&D, and Operations bringing together decades of experience.
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.
QUALITY ASSURANCE
AAPS Consulting can assist your company in planning, implementing, and maintaining a quality system to meet GMP and regulatory compliance in all areas of the product lifecycle. Our services include various quality support such as SOP development, documentation review, change control management, deviation investigation, CAPA support, stability studies, and validation support. With our extensive working knowledge of pharmaceutical regulations and guidelines, we help clients to implement effective and compliant solutions to their quality related issues.
AUDIT
How well do you know your GMP compliance status of your facility or your suppliers? Are you due for a pending audit with Health Canada or an important stakeholder? Our experienced consultants can assist your organization by identifying areas of improvement and potential compliance risks with you or your vendors’ facility and quality system to ensure your organization or vendors are GMP compliant and audit ready.
ESTABLISHMENT AND SITE LICENCE
Before your facility in Canada can manufacture, package, test, label, import, distribute, or wholesale a drug product, natural health product, or medical device, you are required by Health Canada to have a licence for your site or establishment. Our team of experts at AAPS can provide guidance and support to help you navigate the application process to successfully get your site licenced to operate in Canada.
PRODUCT LICENSE
AND MARKET AUTHORIZATION
In order to sell a drug product or a natural health product in Canada, the products must be authorized by Health Canada and labelled with a Drug Identification Number (DIN), a Natural Product Number (NPN), or a Drug Identification Number for Homeopathic Medicine (DIN-HM). These numbers let the public know that the product has been approved by Health Canada to be sold on the Canadian market. Our team of experts at AAPS can assist with your product registration application and ensure it is compliant with Health Canada requirements.
R&D
We have various industry experts to provide their expertise and critical thinking to support with your R&D needs at every stage of the product. Our highly experienced team with years of experience in analytical laboratory operations can assist with your method development in accordance with industry standards. Your intellectual property is secure and any test methods we develop remains within your ownership.
TRAINING
AAPS offers a wide range of highly customizable corporate training solutions to meet your organization’s needs and operation. As a recognized college approved by the Ministry of Training, Colleges, and Universities, AAPS has a proven track record of producing many successful industry professionals in the pharmaceutical, cosmetics, cannabis, and food. Our training courses, seminars, and workshops are taught by our passionate instructor who are industry experts in their field.
OUR PROCESS
Quality & GMP
GMP & Quality
Systems
Documentation &
SOPs
Laboratory Quality
Systems
Laboratory Quality
Documents
Investigation &
CAPA
Stability
Regulatory
Inspection & Audit
Regulatory Submissions
Market Authorization
Establishment &
Site Licensing
Post-Market
Changes &
Approval
R&D
Clinical Research
& GCP
Drug Safety &
Pharmacovigilance
Laboratory
Testing
Method
Development &
Validation
Human Resources
Executive
Staffing
On-Site &
Virtual Training
Professional
Development
Recognized
Certification
