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August 15, 2016
The GMP-certified facility will produce TruTag microtags for global pharmaceutical customers.
August 02, 2016
Regulators and manufacturers address economic and ethical issues for scarce medicines.
Airlines, airports, freight forwarders, and other cold-chain partners are taking a crash course in pharma cGMPs.
Recent revisions to the European Union’s good distribution practices, which were updated in 2013, reflect increased regulatory focus on the supply chain.
August 01, 2016
Planning ahead is key to enabling a continuous and secure supply chain that adapts to changes in market demand.
Now past the “wait-and-see” standoff, most pharmaceutical companies and their contract partners are considering long-term requirements, including distributors’ needs.
The author reviews some of the key considerations when selecting a vendor and crucial parameters that must be defined in the tech-transfer process to ensure the greatest chance of success.
Training and mock audits are the key to preventing data integrity issues with partners offshore, but the process must start at home. Compliance consultant John Avellanet shares best practices and ways to minimize costs.
July 22, 2016
Zenith appointed Carlos Machado as serialization director to lead the company’s sales, operations, and post project support services.
The company opened a new service center in San Juan, Puerto Rico.