Plant monitoring system

Recipharm’s three-year serialization program began in January 2016 and involves a 40-million-euro investment.

Jul 26th, 2010

Hp 19425 Veriteq View Linc

• viewLinc 3.5 is fully validatable for FDA-regulated, GxP-compliant environments, providing continuous records, 24/7 alarming, and automated reporting

• easily deployable for monitoring temperature, RH, CO2, differential pressure, and more

• for larger pharmaceutical packaging plants and medical product packagers, Web-based system provides access for multiple facilities worldwide

Veriteq, a Vaisala company

Veriteq, a Vaisala company

Fda Hi Res Copy

Saleable Returns Verification Delayed to 2023

Additional three-year delay: FDA guidance says distributors will not be required to verify the product identifier of returned drugs before resale until Nov. 27, 2023.

Gavel 5efd2dbada95c

Cannabis Policy Vote May Happen by End of 2020

The MORE Act would be historic in that it would remove cannabis from the Controlled Substances Act, opening a path for regulations to follow.

Alignment 90 Sep Oct 2018

Live from PDA/FDA: FDA Considers Incentivizing Quality Management Maturity (QMM)

The Agency is soliciting feedback from manufacturers on assessing and rewarding QMM through Oct. 2020. Reduced audit frequency may one day be an incentive for high performers.

C Ph I Fo P On White With Dates

CPhI Festival of Pharma 2020 in October

Former FDA commissioner Dr. Scott Gottlieb to address industry on sustainable innovation at the two-week long event. Sessions will cover affordable medicines, supply change resiliency, AI, Vaccine production, and more.

Smithers tests med devices

Smithers, a leading provider of testing, consulting, information, and compliance services, has announced the formation of the Medical Device Testing division.

Med Devices and the FDA: Extended Deadline, Worker Safety

In extending UDI compliance dates for low-risk products, FDA cited challenges related to COVID-19. CDRH also issued recommendations for personnel safety in med device manufacturing.

FDA Commissioner Dr. Stephen Hahn

New FDA Insight Podcast on Emerging Topics

First guest: FDA commissioner Dr. Stephen Hahn on fighting COVID-19 at FDA.

Quick Hits: Allergan is Seeking Women with Recalled Breast Implants

Allergan recalled breast implants more than 10 months ago; now they are trying to find the women who still have them.

Fitbit Ventilator

Quick Hits: FDA Gives Emergency Approval to Fitbit’s Ventilator

The wearable tech company developed a new ventilator to help treat the current health crisis.

Getty Images 1127958533 Drug Prices

States Focus Legislation on Prescription Drug Costs

Though attention has turned to COVID-19, state legislatures were already pivoting away from last year’s opioid legislation to address drug prices—an issue that requires the Healthcare Distribution Alliance to engage across all 50 states.

Getty Images 116406615

Take PDA's COVID-19 Survey in Pharmaceuticals

The Parenteral Drug Association (PDA) is conducting an important assessment to understand industry impacts on operations and supply chains.

Honeywell Bigfinite Collaboration 300 Dpi

Honeywell Collaborates With AI Specialist Bigfinite to Speed Medical Therapies

The collaboration will focus on helping biotech and pharma industries understand and make use of artificial intelligence and machine learning to enable faster development.

World Health Organization (WHO) declared the Wuhan coronavirus outbreak a global health emergency.

W.H.O.: Global Emergency Declared as Wuhan Coronavirus Spreads

Most of the 8,000 cases have been reported in mainland China.

Feds Say Not Legal, But Still It’s Not Rare: Why’s CBD for Sale Everywhere?

In our column’s continuing effort to correct common misconceptions about packaging law, this month we turn to cannabidiol, or CBD.

Un Pac Ked Podcast Graphic

Cannabis Packaging: Don't Fear the Reefer

UnPACKed with PMMI Podcast breaks down the latest developments in cannabis packaging as more and more states open the door to legalization.

Controversial new labeling idea

Headlines from the U.K. sound promising but reading deeper reveals very little benefit for contemplating such a major change for food manufacturers.

Activ-Blister Packaging / Image: Aptar

FDA Approves Activ-Blister™ Packaging for HIV Drug

The FDA has approved AptarGroup’s packaging solution for oral solid dose HIV prevention medicine.

Holographic foils can be used to great effect to differentiate product at the point-of-sale.

Using Holography to Fight Pharmaceutical and Healthcare Brand Piracy

Column: New trends in pharma packaging follow developments in emerging markets, demographic changes and new technologies that include holography, says chairman of the International Hologram Manufacturers Association.

Baby Powder / Image: Flickr

FDA Finds Asbestos in Baby Powder, Recall Ensues

Johnson & Johnson recalled thousands bottles of their famous baby powder after the FDA found trace amounts of asbestos.

Yourway Mitigates Uncertainty of Brexit for Clinical Trials in Europe

Their new location is strategically placed to accommodate both the UK and mainland Europe.

More in Regulatory

Digital Network Platform to Further Transform the Global Pharmaceutical Supply Chain

TraceLink: Digital Network Platform to Further Transform the Global Pharmaceutical Supply Chain

The platform is designed to allow users to rapidly design and deploy network orchestration and analytics applications, enabling patient-centric orchestration across the end-to-end life sciences value chain.

Schreiner MediPharm's Flexi-Cap Prime has a combined tear strip for the label and cap

Schreiner MediPharm: Tamper-Evident Flexi-Cap Prime for Vials

The tear strip is designed to ensure that undetected reuse of a container is no longer possible.

Duane Niedert, Director of Operations – Americas for Smithers

Smart Packaging: ‘A Tale of Two Technologies’

A presentation at SmartPack 2019 delves into the current status, forecast, and drivers of the two categories of technology—smart and active—that make up smart packaging.

Migrane Drug Needed / Image: Getty

FDA Approves New Acute Migraine Drug

Eli Lilly’s new drug Reyvow relieves pain, nausea, and light sensitivity in within two hours of ingestion.

Descovy / Image: Gilead

FDA Approves HIV Drug, But Only for Men

Gilead Sciences only tested Descovy on men and transgender women, and the approval explicitly excludes cisgender women.

Zantac and generic versions of the popular heartburn medicine face concerns about contaminants.

How QR Codes Can Help Drug Makers Streamline Recalls

Concerns about a carcinogenic impurity have prompted recalls of Zantac and generic versions of the popular heartburn medication. Smart labeling technology could speed and clarify alerts to consumers and also help drug companies reduce scrapped lots.

Infant Werewolf Syndrome / Image: Shutterstock

Mislabeling Leads to 17 Cases of Infant “Werewolf Syndrome”

Children in Spain have developed hypertrichosis after a reflux drug was contaminated with alopecia treatment.

Visible Particulate FDA Recall Notices by year as compiled by John Shabushnig, Insight Pharma Consulting, from FDA data. Reprinted with permission.

Particles in Parenterals: 2019 Update

FDA expects a visual inspection program and parenteral manufacturers should expect questions about their program during any inspection. What's new in 2019?

Toshiba’s new thermal barcode printer, the B-EX4T3HS, prints at 600 dpi at speeds up to 6 in/s.

High-Precision Printer Eases Compliance in Medical Packaging

Toshiba’s latest thermal barcode printer combines high-resolution printing with high precision in label feeding to print small labels.

Opioids / Image: iStock

FDA and DEA Target More Illegal Opioid Websites

In the continued fight against the opioid crisis, the FDA and DEA issued joint warning letters to websites illegally marketing and selling opioids.

Digital Brand Protection: Fingerprinting for Serialized and Non-Serialized Products

Systech’s next-generation platform is a brand protection suite that integrates fool-proof product authentication with serialization, traceability and insight.

NUsurface Meniscus Implant / Image: Active Implants

First Artificial Meniscus is an FDA Breakthrough Device

The FDA has designated the first artificial meniscus implant a breakthrough device, expediting its review process.