Building a high level of knowledge to maximize the efficiency of pharma manufacturing process

Plant managers will need to hone many skills that include: technology, regulatory and compliance, health economics and how to be a facilitator to technologies that allow levels of access and process customization that were previously inconceivable.

Check out the agenda

GOOD DISTRIBUTION PRACTICES

27 October - 28 October

Regulatory impact from procurement to the client

Industry Session - Maximizing efficiency: Process Analytical Technologies and Process Intensification

27 October - 27 October Montjuïc, Hall 5, Area Palau de Congressos de Barcelona, Room VIP Room

Process Intensification -reduction of unit operations by replacing traditional segmented processes by high-end integrated processors- and Process Analytical Technologies -taking the analytical capabilities from the lab to the production process- pave the way to higher holistic levels of efficiency in the production of pharmaceuticals.

GDP. What is the impact to the API manufacturers?

27 October - 27 October Montjuïc, Hall 5, Area Palau de Congressos de Barcelona, Room VIP Room

GDP. What is the impact to the distributors?

27 October - 27 October Montjuïc, Hall 5, Area Palau de Congressos de Barcelona, Room VIP Room

GDP. What is the impact to the FDF manufacturers?

27 October - 27 October Montjuïc, Hall 5, Area Palau de Congressos de Barcelona, Room VIP Room