Global Regulatory Services (GRS) is a 'one stop shop' for regulatory affairs and quality compliance within the life sciences sector and with our global network of independent advisers and consultants we can offer regulatory affairs advice and solutions to companies throughout the World. From the outset we have provided our clients with ‘on the ground’, country-specific knowledge. We have found it invaluable to have these local contacts in order to maximise the chance of a successful outcome in terms of a client’s regulatory strategy and/or licence submission.
Our extensive portfolio of services includes assisting companies with their regulatory strategy and product development; Traditional Herbal Medicines Registration Scheme (THMR); pharmacovigilance; development of medical, diagnostic and pharmaceutical devices (from concept generation to manufacturing support); general regulatory assistance and involvement with innovative technologies.
With the Pharmaceutical Industry constantly changing through re-structuring, mergers, acquisitions and new regulations, we have first hand experience of regulatory functions becoming strained because of lack of resources. If there is a tight deadline to meet, a complex project or even a simple variation to undertake by outsourcing to Global Regulatory Services, our clients will be able to achieve their business objectives safe in the knowledge that we will deliver.
We also welcome the opportunity to work with individuals and companies who are involved in the development of new and innovative technologies.
We are comfortable at working at all levels from administration through to the boardroom with clients ranging from biotech start-ups to multinationals.
Please contact us via email - GRS@globalregulatoryservices.com - we are here to help.