Offering you practical solutions with outstanding results, NSF International provides a range of high-quality support services to the global pharmaceutical industry. This includes world-class regulatory and pharmaceutical compliance consulting, auditing and training including public, on-site and online training.
The objective of NSF's pharma team is to provide you with the best customer service available and to help you achieve your goals. Our customised education programs are designed to change behaviors and improve workplace practices, not just to pass on information.
Our pharmaceutical compliance consulting and auditing services have one objective in mind: to help improve your productivity (efficiency and profit) and regulatory compliance. Unless you achieve both, you will go out of business.
Our unique combination of former regulatory agency staff and experienced industry professionals can provide specialist knowledge and expert advice. Contact us if you want to be proactive and drive improvements, or if you have some specific pharmaceutical regulatory or technical issue and need guidance.
Our pharmaceutical and biotech consultant team can help you develop and implement a cost-effective, compliant pharmaceutical quality system, provide advice on the design, qualification and validation of new facilities, equipment, computerized systems and processes, and help simplify quality processes, SOPs and batch records. We can also help you benchmark against best industry practices (beyond the regulations).
Let our pharmaceutical auditor support team take a close look at your facilities and operations. Our team of pharmaceutical auditors can perform audits against Good Manufacturing Practice, Good Distribution Practice, Good Pharmacovigilance Practices and Good Clinical Practice international regulations and standards.
We can audit active pharmaceutical ingredients, excipients, medicinal product manufacturers, distributors, investigational medicinal product manufacturers, QC laboratories, affiliate contract manufacturers, computerised systems and more.
Our pharmaceutical auditing processes can be tailored to your specific needs. This includes due diligence audits, auditing your supplier or internal audit processes, compliance auditing, assessing activities against standards, inspection readiness audits and more. Outputs can include efficiently reaching compliance.
We provide customised on-site training, public pharmaceutical courses and eLearning. You are only as good as your people. NSF offers education programs that will change behaviors, improve performance and "future proof" your organisation. Any of our short public pharmaceutical courses can be tailored and run on-site.
Whether you are looking to send one of your people to a public pharmaceutical course for career progression (including becoming a Qualified Person), to train many employees economically through pharmaceutical eLearning, to train a group of staff in house in changes in procedures and regulations, or to bring about culture change within an entire organisation, we have the skills and programmes to meet your needs.
Examples of education offered annually include Good Manufacturing Practice including clinical trials, regulatory issues and regulatory affairs, auditing and self-inspections (A CQI and IRCA certified course), sterile and biotech products manufacture training, human error and behavioural GMP training.
We also work alongside the University of Strathclyde to provide a Royal Society of Chemistry Approved Qualified Person training program. More people have become QPs in Europe through our training programme than any other training provider, so you can rest assured you're in good hands.
Please use the form below to send us your enquiry, or if you have specific questions don't hesitate to contact us via firstname.lastname@example.org.