Working with our affiliated product development global teams as a co-development partner, PHARMACARE PREMIUM can optimise complex development processes by seamlessly integrating formulation, validation batch production, bio-equivalency studies, as well as all regulatory processes leading to registration of products to fully scaled up production, and where relevant to ensure strategic stock and pile execution.
Pharmacare Premium offers contract development services ranging in scope from formulation and analytical method development and validation to BE and submission batches.
Pharmacare Premium will project manage the whole process according to pre-agreed timelines and milestones including sub-contracted services at either Pharmacare Premium’s or the Customer’s partners.
At Pharmacare each activity undertaken is a project to be managed and each process is a progression to be bench marked and reviewed against exacting performance metrics.Our departments are focused towards a common purpose, at the heart of which are our commitments to our clients.
All our processes deliver with industry compliance as our framework and premium quality as our standard.
The unique patent position of Malta makes such development activities much more cost effective with a faster return on investment and wider possibilities of early launches. The scope of related activities includes:
– PROJECT MANAGEMENT
– BIOEQUIVALENCE BATCHES
– SUBMISSION BATCHES
– STABILITY STUDIES
– REGULATORY SUPPORT