Butterworth Laboratories: Science on Demand
Butterworth Laboratories mixes highly qualified, experienced analysts with cutting-edge technology, add in market-leading quality systems...
At Butterworth Laboratories Ltd we understand the importance of keeping up with changes in the Pharmacopoeias and ensuring their implementation. A revision of USP, Residual Solvents.
The revision clarified verification and validation requirements for use of the monograph for Class 1, 2, and 3 residual solvent determination in compendial materials. In addition, as part of the revision, USP <1467> was introduced to delineate verification and validation requirements. Both became effective from 1 March 2019.
Butterworth Laboratories mixes highly qualified, experienced analysts with cutting-edge technology, add in market-leading quality systems...
Butterworth Laboratories is pleased to announce that it is undertaking a complete laboratory development as...
In early 2020, Butterworth Laboratories Ltd (Butterworth) were eagerly anticipating a letter from the MHRA...
One of the most discussed topics currently affecting good manufacturing practices (GMP) laboratories, data integrity...