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Scientific Insight Enables Risk Mitigation: Why West is By our Customers’ Side
As regulations increase across the pharmaceutical industry, reliable scientific evidence is needed to support the decisions being made during the drug development process in order to achieve the safe delivery of medicines to patients.
Recent regulations around issues such as particulate and heavy metals, require a strong understanding of the testing and analysis to move drug products to the market.
Collaboration with strategic suppliers is critical to managing issues associated with bringing a sensitive drug molecule to market. By supporting our customers from molecule to market, West works to build a close partnership that can provide the scientific analysis, data and regulatory support needed to mitigate risk, speed drug development, and get drug products to market to support patient health.
No matter what challenges our customers face during the drug product life-cycle, chances are West has faced them before. With nearly a century of industry leading experience, West may already have the answers you need, and if not, we can develop a scientific approach to find what you’re looking for. Working together, we can address issues quickly and effectively, helping to mitigate risks as early as possible in the development process by helping customers navigate regulatory and technical challenges.
To learn more about how West can help, check out our video here on our Integrated Solutions Program page.#WestByYourSide
It is imperative for the pharmaceutical industry to be prepared to comply with new compendia chapters as soon as they are enacted. This comprises both knowing of proposed changes as soon as announced and being well prepared to accommodate them. USP Chapter <381> is changing, and Chapters <382>, <1382> and <1381> are being created. The Pharmacopeia Forum for final comments has been published.
In 2017, West employees have worked diligently to help the communities in which we live and work. Through West without Borders, West's employee-led giving program, employees have raised more than $3 million for a variety of charities around the world.
On March 18 in NYC, West Pharmaceutical Services, Inc. was recognized as a leading Contract Manufacturing Organization (CMO) among emerging biotech companies (EBT) at the <a href="http://cmoleadershipawards.com/index.php"><span style="text-decoration: underline;">2015 CMO Leadership Awards</span></a>.
<p>We are proud to announce our inaugural Corporate Responsibility Report. West’s commitment to sustainability and remaining active in the areas where we live and work are integral to West’s culture. In Parts 1-3 of this five-part blog series on the report, we focused on West’s efforts in <a href="/blog/2017/june/corporate-responsibility-for-2016">Compliance and Ethics</a>, <a href="/blog/2017/july/corporate-responsibility-report-part-2-philanthropy">Philanthropy</a> and <a href="/blog/2017/july/corporate-responsibility-report-part-3-celebrating-diversity">Diversity</a>.</p><p>The fourth part of the five-part series on West’s Corporate Responsibility discusses West’s Health and Safety programs.</p>
<p>The right seal is essential for proper drug product vial closure. West offers a wide range of Flip-Off<sup>®</sup> seal (FOS) products to meet customers’ varying requirements. Three grades are available for crimping needs in varying environments:</p><ol><li>Standard Flip-Off<sup>®</sup> seals: for consistent, reliable crimping outside controlled environments</li><li>Flip-Off<sup>®</sup> Plus seals: for clean crimping under grade A air supply</li><li>Flip-Off<sup>®</sup> Clean, Certified, Sterilized (CCS) seals: for aseptic crimping inside grade A environments.</li></ol>