Integrating up-to-date training programs for all areas of business is essential for a company’s overall success. PharmEng Technology provides international consultation and training for all essential aspects of healthcare industry compliance, including regulatory affairs. With the help of the proven expert training staff PharmEng employs, companies can manage the skills of personnel and meet the standard compliance expertise needed for their unique business.

Training for compliance with Good Manufacturing Practices (GMPs) and governmental regulatory affairs’ world-wide, is comprised of four specific courses within the Regulatory Affairs Training Course:

  • Medical Devices
  • Medical Devices
  • Nutraceuticals
  • Biotechnology
  • Pharmaceutical

PharmEng Technology is a global compliance consulting firm that has excelled for 15 years in helping clients all around the world with their experience, knowledge, and technologically advanced tools – to meet all compliance needs and create a stable training program for sustained compliance. By taking a step toward compliance and using our services to integrate advanced training programs into your business or industry, a foundation of sustainable compliance is built creating innovation and growth.

With projects all around the world and offices in USA, Canada, and Asia; PharmEng Technology has a proven track record of success in helping clients in find compliance solutions inside our highly regulated industry. Our training combines the insights gained from a diverse and able world-wide staff and perfected delivery with effective applications for optimal knowledge retention. We’re confident in guiding you through the application suited for the small or large organization you’re needing compliance solutions for.

Within the healthcare industry we’ve successfully served for over 15 years, there’s a highly stringent regulatory standard to comply with, as we know. Solutions in dealing with compliance become more complex with the constantly changing regulations and laws, which means a system of training with our resources is essential in maintaining up-to-date compliance standards. By organizing a strategy with our consultants, a training program could be developed suited for the specific needs of your business.

Risks of non-compliance will drastically reduce when our training programs are used, which can ensure cost-savings alone in addition to effort and time savings. Implement a training system with our materials at specific intervals to meet standard regulatory affairs compliance, and let our pharmaceutical regulatory affairs experts do the work for you. To learn more, contact us and we’ll be glad to help.