Indoco’s AnaCipher CRO clears US FDA inspection with Zero 483s
The CRO, located in Hyderabad, was inspected by the FDA from 12th to 16th September, 2022
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Anacipher
Indoco’s CRO AnaCipher receives UKMHRA accreditation
A virtual inspection was carried out from 4th to 7th May and 10th to 11th May, 2021
Indoco’s Clinical Research Organisation receives zero 483s from US FDA
The company also recently successfully concluded an audit by US FDA at its sterile manufacturing facility in Goa (Plant II)
Indoco’s CRO – AnaCipher clears US FDA inspection with ZERO 483
The inspection successfully concluded without any observations and no form 483 is issued