Latvian drugmaker JSC Grindeks (GRD1R: RI ) says it has successfully passed a US Food and Drug Administration inspection of its manufacturing facilities, paving the way for Grindeks’ cooperation with the US partners, and developing its business activities on the American market.
The certification allows Grindeks to start exporting its manufactured xylazine, xylazine hydrochloride and droperidol to the USA, as well as continue supplying oxytocine and detomidine to its American partners.
Grindeks chairman Juris Bundulis commented: “This successful achievement gives Grindeks» new development opportunities and strengthens its position on the global pharmaceutical market, as the US Food and Drug Administration approval is a convincing argument to gain the trust of every client. We are proud of our achievements in manufacturing and quality control and are looking forward to new export opportunities.”
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze