API Synthesis

Our Capabilities Include:
<ul>
<li>cGMP compliant, multifaceted facility with fully validated equipment and Part 11 compliant distributive control system</li>
<li>Delta V monitoring of reactos parameters, facility utilities and USP water system</li>
<li>Large scale tangential flow filtrations (TFF) expertise and capability</li>
<li>20L and 200L lyophilizers</li>
</ul>

We offer cGMP synthesis and purification of bio-organic intermediates, excipients and bulk actives. With more than 30 years of experience and expertise in custom APIs scale-up and manufacturing for both pharmaceutical and biologics, we can effectively support your needs for: 
<ul>
<li>Polyamino acids including Poly-L-Lysine and others</li>
<li>Carbohydrates</li>
<li>Lipids</li>
<li>Detergents</li>
<li>Buffers</li>
<li>Custom processes derived from a variety of plant derived natural or synthetic sources</li>
</ul>

<h2>Offering you a world of capabilities</h2>
The global footprint of our API contract manufacturing services assures you of wide-ranging <a href="/US/en/life-science/quality-and-regulatory-management">regulatory and supply expertise</a>, easily accessed through a single trusted partner.
Our API Contract Manufacturing Facility Locations
<ul>
<li>Buchs, Switzerland (cGMP)</li>
<li>Madison, Wisconsin (cGMP) </li>
<li>St. Louis, Missouri (cGMP)</li>
<li>Schaffhausen, Switzerland (cGMP)</li>
</ul>

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Our API contract manufacturing services can support all stages of your project. Partner with an industry leader offering a global footprint and decades of experience for your drug development and manufacturing, leveraging our dedicated team and broad product portfolio with single-point project management.

Services

Contract Manufacturing

Complex APIs