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 one-on-one video interview between our editorial teams and industry leaders.
Listen to expert discussions and interviews in pharma and biopharma.
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.
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?
Stability storage services added to Velesco's development offerings.
April 29, 2011
By: Tim Wright
Editor-in-Chief, Contract Pharma
Velesco has partnered with stability storage provider Vindonwestech, Inc. to enhance its drug formulation development program and clinical trial manufacturing services. Velesco supports early stage drug development projects from two locations in Plymouth and Kalamazoo, MI with contract analytical and drug formulation services, as well as cGMP clinical supplies for non-sterile dosage forms. Vindonwestech, Inc. provides services for both CROs and pharmaceutical manufacturers, facilitating cGMP storage of biological and pharmaceutical materials over a wide array of temperature and humidity. Vindonwestech also designs, manufactures and installs a wide range of standard and custom controlled environment room systems, validated to meet the demanding requirements of the pharmaceutical, medical, biological and healthcare industries. Patrick Jackson, director of Vindon, commented, “Vindonwestech is pleased to be associated with Velesco as Vindonwestech is particularly committed to providing storage services and equipment strengthening Velesco’s ability to deliver a first class stability program.” Shirley Smith, Quality Assurance director at Velesco noted, “the Vindonwestech facility is impressively designed and equipped. A Velesco and Vindonwestech collaboration assures a strong cGMP quality program and clients can be confident their clinical trial materials will exceed FDA compliance requirements.”
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 !