Explore recent issues of Contract Pharma covering key industry trends.
Read the full digital version of our magazine online.
Stay informed! Subscribe to Contract Pharma for industry news and analysis.
Get the latest updates and breaking news from the pharmaceutical and biopharmaceutical industry.
Discover the newest partnerships and collaborations within the pharma sector.
Keep track of key executive moves and promotions in the pharma and biopharma industry.
Updates on the latest clinical trials and regulatory filings.
Stay informed with the latest financial reports and updates in the pharma industry.
Expert Q&A sessions addressing crucial topics in the pharmaceutical and biopharmaceutical world.
In-depth articles and features covering critical industry developments.
Access exclusive industry insights, interviews, and in-depth analysis.
Insights and analysis from industry experts on current pharma issues.
A detailed look at the leading US players in the global pharmaceutical and BioPharmaceutical industry.
Browse companies involved in pharmaceutical manufacturing and services.
Comprehensive company profiles featuring overviews, key statistics, services, and contact details.
A comprehensive glossary of terms used in the pharmaceutical and biopharmaceutical industry.
Watch in-depth videos featuring industry insights and developments.
Listen to expert discussions and interviews in pharma and biopharma.
Download in-depth eBooks covering various aspects of the pharma industry.
Access detailed whitepapers offering analysis on industry topics.
View and download brochures from companies in the pharmaceutical sector.
Explore content sponsored by industry leaders, providing valuable insights.
Stay updated with the latest press releases from pharma and biopharma companies.
Explore top companies showcasing innovative pharma solutions.
Meet the leaders driving innovation and collaboration.
Engage with sessions and panels on pharma’s key trends.
Hear from experts shaping the pharmaceutical industry.
Join online webinars discussing critical industry topics and trends.
A comprehensive calendar of key industry events around the globe.
Live coverage and updates from major pharma and biopharma shows.
Find advertising opportunities to reach your target audience with Contract Pharma.
Review the editorial standards and guidelines for content published on our site.
Understand how Contract Pharma handles your personal data.
View the terms and conditions for using the Contract Pharma website.
What are you searching for?
Will manufacture, distribute more than 100 products while continuing remediation
January 23, 2013
By: Gil Roth
President, Pharma & Biopharma Outsourcing Association
Ben Venue Laboratories, a Boehringer Ingelheim subsidiary, has voluntarily entered into a consent decree with the FDA relating to its GMP requirements. Under the terms of the consent decree, BVL is permitted to continue to manufacture and distribute more than 100 “important drugs that are essential for patient care,” according to a company statement. The company conducted both contract manufacturing and generics business (as Bedford Laboratories) through the Bedford, OH site. Doxil, a key cancer drug from Johnson & Johnson that was manufactured by BVL is in the process of being transferred to another contract manufacturer. In its earnings call yesterday, a J&J spokesman, said that the company has “made significant progress to restore a reliably supply [of Doxil]. An alternate manufacturing approach consisting of a collaboration between [BVL] and another supplier to complete end-to-end production of Doxil was approved in the EU and Japan late in 2012 and in Canada earlier this month.” The U.S. supply of Doxil, also manufactured by BVL and a second CMO, was restored fully in October 2012. BVL is permitted to continue drug-development activities, and may file abbreviated new drug applications (ANDAs). If remediation progresses to the FDA’s satisfaction, it may receive ANDA approvals and manufacture other products. The consent decree is subject to approval by the U.S. District Court for the Northern District of Ohio. So far, BVL has spent more than $300 million to upgrade its facilities, making improvements and changes to processes to address the manufacturing-related issues that resulted in the company’s decision to voluntarily halt manufacturing in November 2011. An FDA inspection in May 2011 resulted in a 33-page 483 Warning Letter, while the FDA’s most recent inspection in November-December 2011, led to 10 separate cGMP deviations. The company has worked steadily to improve its manufacturing processes, and announced in October 2012 that limited production had resumed. Since that time, production has resumed on additional manufacturing lines.
Enter your account email.
A verification code was sent to your email, Enter the 6-digit code sent to your mail.
Didn't get the code? Check your spam folder or resend code
Set a new password for signing in and accessing your data.
Your Password has been Updated !