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Wasdell’s commitment to Quality and adherence to the highest standards of GMP (Good Manufacturing Practice) is Total. As an audited and approved Supplier to the major Pharmaceutical, Neutraceutical, Vitamin, Veterinary and Healthcare Companies, we pride ourselves on the hard earned reputation we have developed with our business partners.
The Company is committed to a process of continual improvement and comply with current GMP standards as set out in “Rules and Guidance for Pharmaceutical Manufacturers and Distributors 2002” (The Orange Guide).
To achieve our goals Wasdell Packaging Limited maintain an effective and reliable Quality System which is planned, reviewed and maintained by the Management Team.
Controls and checks are carried out at all stages of the Production process by our highly experienced Quality Assurance Team who cover all aspects of the Quality Assurance Procedures.
All product, components and packed stock undergo strict quality checks throughout the process to ensure that all orders are completed to the Customer’s satisfaction and in accordance with the Product Licence.
The MHRA has granted licence No ML/1411/1 to Wasdell in the following categories:
- Manufacturing (Assembly only). This covers Blister Packing, Tablet/Capsule Counting and Filling and also Secondary Packing/Hand Assembly.
- Investigational Medicinal Products Manufacturing Licence. This covers the packing of solid dose formats for Clinical Trials.
- Specials Manufacturing Licence.
To help provide a comprehensive Quality Service, Wasdell can also provide QP Release and Regulatory Support.
Wasdell Packaging Limited can also pack to the FDA Standard. This Customer driven capability is available for product specific orders.
Wasdell also hold a MAIMP Clinical Trial Licence.
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WASDELL PACKAGING
LTD |
“PUTTING
CUSTOMERS FIRST” |
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