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Method Development and Method Validation Using HPLC, GC and GC-MS

LPD Lab Services have experienced members of staff with a history of developing chemical analytical methods for drug substances (API) and drug products as well as impurity forced degradation studies and excipient assays within the Pharmaceutical industry.

The same analytical chemistry approaches have been applied to manufacturers of polymers, medical devices, cosmetics and chemicals as well as a range of other industries.

LPD Lab Services are able to validate analytical methods developed in-house, client supplied methods or published methods.

The laboratory can use HPLC, GC, GC-MS or a range of other chemical analyical techniques in its method development and method validation activities.

Our site experts on chemical method development and validation are Wyndham Johnstone and Adam May.

Please contact us to discuss how your requirements can be met using. We can issue no-obligation quotations once we have discussed your needs and can offer two levels of service “urgent” and “normal”. We also offer preferential rates for longer term analysis contracts.
 

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