cGMP Contract Manufacturing Service

Rutland Biodynamics is licensed by the MHRA (Dept. of Health) for the pharmaceutical manufacture of liquid and semi-solid preparations under cGMP conditions (MIA 28255) Click here for copy of GMP Certificate. We are able to manufacture a wide range of batch sizes, from small up to medium-large scale, depending on method requirements.

We also supply QP services for products manufactured here.

We are qualified to offer Supplier Approval audit services at home and abroad.

We are pleased to be able to offer cGMP contract manufacture, as well as bottling and labeling services, either for customer’s own products or using the high quality organic herbal medicines made fresh from our own fields, all supplied in environmentally efficient
and recyclable packaging.

Since 2006, we have been involved in developing licensed herbal medicinal products (traditional herbal registrations or THRs, herbal medicines licensed for retail sale under 2004/24/EC) which other ‘own-label suppliers’ can market to sell ‘over-the-counter (OTC) in the UK. These are made using either our own-grown herbs or from raw material ingredients supplied from other approved sources.
Some of these are also used as ingredients in products finished overseas. We are also retained by clients to develop their own THRs.

We also make a number of special cGMP ingredients, such as extracts, tinctures, mixtures, creams and ointments for others to finish or to incorporate in other ‘own label’ brands.

An important part of our business is the contract manufacture of liquid and semi-solid licensed medicines (PLs) or ingredients (APIs) for other licence owners.

cGMP laboratory analyses are carried out on site with an ever increasing range of specialised skill and sophistication.

If you are interested in this or would like to find out more, please contact us.