Over the past five years, the cosmetic industry has met with several legislative changes. Within the new legislative package, including the new REACH and CLP, it is important to find a comfortable routine that will minimize costs while staying effective and compliant with all regulations.
Tips for the Shipping Process of Pharmaceuticals and Biologics
Find out how to simplify the shipping process for temperature-sensitive pharmaceuticals and biologics and how to contain cost when shipping bulk pharma and biologics.
A new approach to one-way universal shipping has made it far more convenient to send temperature-sensitive healthcare packages. Key changes in package design allow you to forget the pains of bench-time (or sweat time). What’s more, SKU management is simplified with four payload sizes to choose from where each size makes use of the same components and the same pack out is used for both 3-day and 5-day shipments.
Watch this video to see how a few innovative changes in package design can radically improve your temperature-sensitive packaging operations.
In this video podcast, Ben VanderPlas, Global Product Manager at ThermoSafe speaks with Jim Chrzan, Group Publisher of Healthcare Packaging providing insights into the below topics as it relates to ThermoSafe’s latest innovation – LD7 QPMC pallet shipper.
Learn more about the QPMC pallet shipper at thermosafe.com/palletsolutions
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Advanced Protein Aggregation & Characterization
This training will focus on occurrence of particles in drug products, effects of protein aggregates, critical process and parameters. Attendees will gain overview of on utility and limits of predictive experiments, learn concerns from the authorities and relevant aggregation guidelines, and more.
CMC Analytical Comparability: Methods & Strategies for Biologics, Biosimilars & Biobetters
Attendees will be introduced to comparability in biosimilar development, the analytical strategies of protein characterization of biosimilars, the structure of proteins, in vitro pharmacology and much more.
Corporate Compliance & Transparency in the Pharmaceutical Industry
This two-day conference will serve as a platform for an open and dynamic dialogue with HCPs and patients to achieve common goals. Learn how to embed compliance in the business and develop one simple system for managing compliance & transparency in a complex and regulated environment.
Driving the national agenda of Medical tourism through PX Excellence
Read the interview with Dr. Layla Al-Marzouqi, Director of Medical Tourism Council at Dubai Health Authority, and learn how to enrich patient experience and quality of healthcare.
No more trouble with dangerous good shipments
Global temperature controlled pharmaceutical shipments are constantly faced with new logistics challenges and regulations. This January 2017, IATA Dangerous Goods Regulations added further complexity to shipping cold chain products compliantly.
5 Changes in Signal Detection Management
The European Medicines Agency, regulatory authorities in the Member States and marketing authorisation holders are responsible for detecting and managing safety signals. A safety signal is generally defined as information about a new or known Adverse Event that may have been caused by a medicine, where it is therefore necessary to conduct further investigation. Evaluation of safety signals plays a major role within pharmacovigilance. Therefore, it is vital for regulatory authorities to know the latest updates detailing the risks and benefits of medicines. The EudraVigilance database is an important source of information on suspected adverse reactions and signals.