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Machinery & Materials
Logistics & Cold Chain
Regulatory: Page 3
Solution for Expiry Labels, DtP, and Study Timelines Due to EU 536/2014 Clinical Trials Regulation
The new regulation improves many aspects of clinical preparation and activation but brings certain new challenges for sponsors.
March 18, 2022
Full Vial Inspection: Simply Complete!
Unit carries out optical and radiometric inspection and volumetric determination of O2 content in the headspace
March 15, 2022
Future for Pharmaceutical Manufacturers Includes More Digitized Data Collection
While automation is driving physical changes to pharmaceutical production and packaging processes, another significant shift is occurring in the accumulation and use of data.
March 14, 2022
Part 1: Manage Challenges from the EU 536/2014 Clinical Trials Regulation
Plan ahead for study startup timelines, expiry labeling on primary packaging solutions, and study administration methods.
March 10, 2022
Tips for Exporting Goods in 2022
Live from Natural Products Expo West: An international trade expert discusses why you need to know your buyers, what you can ship to a sanctioned country, insurance for sea cargo, and more.
March 9, 2022
FDA Issues Voluntary Recalls Final Guidance
The guidance will help companies prepare to quickly and effectively remove violative products from the market, as the agency urges companies to be “recall ready” to protect public health.
March 4, 2022
Industry Reacts to FDA Draft Guidance on Injectable Products Inspection
Pharmaceutical companies and the International Society for Pharmaceutical Engineering want the FDA to align visible particle classifications and inspections with USP.
March 1, 2022
FDA Proposes Rule to Amend Medical Device CGMP Requirements
The proposed amendments to the CGMP requirements of the Quality System (QS) Regulation will align them more closely with the international consensus standard for devices.
February 28, 2022
New FDA Chief Confirmed by Senate
Dr. Robert Califf narrowly secures position again on a 50-46 vote, despite concerns over his pharmaceutical industry ties.
February 16, 2022
GAO Makes Recommendations to Improve FDA Foreign Inspection Program
Drugs manufactured overseas for the U.S. market must meet the same requirements as those manufactured in the U.S., raising questions about the equivalence of foreign to domestic inspections.
February 9, 2022
FDA Proposes Rule for Wholesale Drug Distributors, Third-party Logistics Providers
If passed, the rule would allow only those licensed according to the proposed national standards to engage in transactions related to the sale and distribution of certain prescription drugs with other members of the supply chain.
February 8, 2022
FDA Publishes Draft Guidance on Reporting Certain Medical Device Shortages
The new guidance helps clarify how the agency interprets 506J notification requirements, including when and who should submit a notification and the information that should be included.
February 1, 2022
Page 3 of 188
Q&A: Foil Tariffs Pose Imminent Threat to Healthcare Costs, Lead Times
In this Q&A, we talk with PAXXUS' Dwane Hahn about the serious supply chain continuity implications that loom as the packaging community awaits a scheduled decision from the Department of Commerce on December 15, 2022.
MassRobotics Names Participants in Healthcare Robotics Startup
Quotables and By the Numbers: November 2022
Haleon, Microsoft Enhance Product Accessibility for Vision Impaired
Gel Packs in Recycle-Ready Film
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Discover innovative solutions for packaging and processing, automation, sustainability, e-commerce and more.
RFID Tag Encoding and Logging Solution
The Sato and Loftware cloud-based solution helps producers of medical devices and pharmaceuticals meet stringent traceability requirements.
Tablet Press Solution
Connected Printer Services
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Triumphs and Challenges in Sustainability
Healthcare Packaging News Roundup: Sustainability
Healthcare Packaging's Most Popular Articles
Healthcare's Sustainability Approach: Waste Reduction
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