Women working in the lab

Committed to service excellence

Your success
is our success

As a leading provider of integrated CDMO service solutions for organizations on the cutting edge of drug development, SK pharmteco is driven by a collective goal of excellence in all we in do. We fully engage in giving our best for the benefit of all stakeholders, taking ownership and pride in our work. Our ways of working embody this mission, from our unique approach to program management to systematic technology transfer and deep regulatory expertise and experience.

Seamless technology transfer

While SK pharmteco offers a broad spectrum of custom process and analytical development offerings, we also work closely with partners to transfer their products, processes, and technologies to our facilities for continued development, scale-up, or commercial manufacturing. Whether you’re relying on us for large-scale manufacturing of an API or production of a gene or cell therapy product for clinical trials, our focus on transparent communication and collaboration ensures our partners can feel secure in transferring processes to SK pharmteco.

Leveraging our teams’ deep expertise and technology transfer experience, SK pharmteco is prepared to accommodate a client’s technical requirements to ensure all elements are safely and seamlessly transferred. From proof of concept to product lifecycle management and everything in between, we have the technology and versatility to fully comply with your organization’s tech transfer specifications at any scale.

Raw Material Identification & Characterization with SK pharmteco

Regulatory knowledge and experience are fundamental to a CDMO’s ability to guide partners in navigating regulatory complexity and maintaining compliance at every step of the drug development lifecycle. SK pharmteco empowers clients with a depth of regulatory knowledge that can only come from a legacy of successful engagements with global regulatory agencies.

Our track record of regulatory excellence includes: 

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pre-approval inspections (PAIs) passed over the last decade
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recent PAIs waived
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successful regulatory inspections since 2020
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approved products in production across all sites
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inspection pass rate across all facilities

Contact us

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