LET AAPS INDUSTRY EXPERTS GET YOUR TEAM UP TO SPEED.
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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 TRAINING SERVICES
AAPS is your partner for training services. We offer a wide range of highly customizable corporate training solutions to meet your organization’s needs and operation. For the past 20 years, AAPS has been recognized globally as a leading training institute for the pharmaceutical, food, cosmetic and related applied science industries.
We offer training through courses, seminars, and workshops and they are taught by our specialized instructors who are industry experts in their field
We have access to and work with some of the brightest minds in Quality, Compliance, Laboratory, Safety, Regulatory, R&D, and Clinical – bringing together decades of experience.
Most importantly, AAPS provides customized training solutions to fit your organizational needs. We work side-by-side with your team to achieve operational excellence.
MAINTAIN COMPLIANCE
Regulations are constantly evolving in the industry. In order for employees to stay up-to-date on the latest regulatory changes and best practices, ongoing professional development is necessary to stay compliant.
DECREASE TURNOVERS
Invest in your team to reduce employee turnovers and improve morale. Quality training allow employees to feel valued and inspires commitment to achieve organization goals. Consequently this reinforces company values and employee’s commitment to compliance.
BOOST PRODUCTIVITY
Understanding current regulations helps employees identify key areas of improvement, tackle challenges effectively and solve problems intuitively. Investing in quality training benefits both the employee and the organization.
OUR PROCESS
Quality & GMP
GMP Refresher
Documentation &
Record Keeping
Data Integrity
Annual Product Quality Review (APQR)
Investigations & CAPA
Change Control
Regulatory
Inspection & Audit
Regulatory Submissions
Market Authorization
Post-Market Changes & Approval
Temperature Mapping
Laboratory
Product Development
Quality Control Laboratory Testing
Method Development & Validation
Certificate of Analysis
Equipment Operation
Validation (Cleaning & Process)
Clinical
Global Phamacovigilance
Clinical Trial Monitoring
Medical Devices
Drug Safety
