Pharma Lord provides contract manufacturing for world wide Customers
R & D
Why Pharma Lord for Contract Manufacturing
This includes the entire technology transfer of our customers’ products to our manufacturing facilities, in accordance to their dossier requirements.
At Pharma Lord, we are equipped with stability chambers that enable us to conduct ICH stability studies at long-term, intermediate and accelerated conditions.
In addition, we offers many analytical testing services in compliance with GMP requirements and in accordance with the corresponding pharmacopeia (Eur. Ph., USP).
We can also provide regulatory assistance for the preparation of regulatory dossier documentation.
Our manufacturing facilities have been designed to accommodate the production and packaging operations of non-sterile oral solid dosage forms (tablets, capsules, liquid syrup, sachet and powder suspensions for reconstitution). Our manufacturing site has been constructed to the strictest specifications and in accordance with the principles of current Good Manufacturing Practice as required by the guidelines of the European Union: