Our Services

NHP Compliance provides expert assistance at every stage of a GMP compliance program.

We have a team of full-time, dedicated, diversified, committed, and knowledgeable specialists; our associates are assigned to a given project to meet a client's particular needs. We are able to flex to meet changing project scopes (e.g., tightened timelines, market changes, short-term workforce shortages, etc.).

Our services include:
● Project Consulting
● Audits
● QAP Services™
● Regulatory
● Technical Writing
● Training
● Laboratory
● GMP Booklets

 

 

 

Services
 
PROJECT CONSULTING

NHP Compliance can help your company deal successfully with any size of project, from a large multi-faceted quality initiative to the most specialized task, from the design of a complete quality system through to assistance with its implementation.

Working closely with your staff, we are able to look at your processes objectively to determine your needs and priorities. We tailor our services accordingly using our proven processes and templates to provide a practical, efficient and cost-effective approach to your project. You will receive excellent customer service and benefit from our strong project management skills as we move the project forward in a timely, cost-effective manner.

We are committed to conceiving, developing, and implementing strategies and processes to improve quality and efficiency aligned with your priorities. Our associates' excellent project management skills are complemented by their ability to work with the client in utilizing their systems and their personnel to complete the project.

We offer:
  • Management of large compliance projects
  • GMP for clinical trial materials
  • Health Canada audit corrective action projects
  • Backlog cleanups - stability reports, change controls, deviations, batch, record reviews, etc.
  • Interim QAP Services ™ for fabricators - managing your quality system during periods of growth and/or transition
  • For large compliance projects, if desired, we can identify your priorities and address them in a straightforward, systematic manner using The Quality Plan™
 The Quality Plan™
The Quality Plan™ focuses on your specific quality needs, and ensures:
  • You meet all regulatory requirements so you are proactive and more knowledgeable than any visiting auditing team
  • Improved efficiency in the use of your quality resources
  • Your quality systems are always under control, with the status of ongoing activities readily available at all times
  • Continual quality improvement within well-defined budgets
It provides peace of mind and allows for careful resource allocation and is vital in setting long and short term priorities.

We develop The Quality Plan™ from information gathered in The GMP Gap Analysis. This plan includes actions (quality initiatives) with targeted completion dates for the core GMP quality components. It helps:
  • Detail the long-term roadmap to compliance
  • Prioritize quality activities
  • Address outstanding issues from previous audits
  • Communicate with all parties involved
If you prefer, NHP Compliance can help expedite the implementation of your Quality Plan by corresponding with - and providing ongoing guidance to - a key contact in your company who coordinates the onsite work. We have mentored a number of clients in this manner with great success.

 NHP Compliance Is a Full-Service Company
We can provide expertise and assistance with all aspects of quality and compliance, including auditing, Quality Assurance Personnel (QAP), technical writing, GMP training, regulatory, and lab services.

See Audits for more information about The GMP Gap Analysis™ and our auditing services.

Visit our validation website, www.ValidaPharm.com, for more information on our validation services.