Altasciences’ clinical facilities are dedicated to the conduct of early phase and clinical pharmacology trials in a wide range of therapeutic areas. Strategically located in one of the most ethnically diverse regions of the U.S., our Los Angeles clinic works in unison with our eight other sites to offer an integrated drug development solution from lead candidate selection to clinical proof of concept and beyond.

What you can expect:

• 80,000 square-foot, purpose-built facilities
• Dedicated USP 797 pharmacy
• On-site CAP and CLIA-accredited safety reference laboratory
• PBMC processing site Database of over 55,000 active participants
• 180 beds
• 180 clinical experts
• Renowned industry-wide Asian ethnobridging capabilities

Virtually step inside our L.A. clinic here: Clinic Tour - Los Angeles, California

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You may also be interested in the following:

• Webpages:
  • Our Three Clinical Trial Facilities
  • Clinical Research Services
• Video: Quick Chat With Dr. Dave — Discovering Our L.A. Clinical Site

Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining drug development solutions, whether for a single study or multiple programs, to offer an integrated/synchronized approach to CRO and CDMO services.

With the increased demand for our services, we continue to grow our immunogenicity, PK, oligonucleotide, and biomarker capabilities to complement our robust preclinical, clinical, and LC-MS/MS solutions.

With this expansion, we offer you the following:

✔ Dedicated CL2/CL3 space for handling samples and RG2 materials
✔ Balance room for critical reagent and solution preparation
✔ Extraction space for an additional 50 analysts
✔ Additional benches for sample analysis
✔ Enhanced space for cell culture and flow cytometry services

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Speak with one of our experts to learn more about our service offering.

Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining drug development solutions, whether for a single study or multiple programs, to offer an integrated/synchronized approach to CRO and CDMO services.

Have five minutes? Take a look at these:

• Webpages:
  • Bioanalytical Services
  • Bioanalytical Platforms
  • Top 15 Scientific Resources
• eBook: Key Biomarkers of Immunomodulators: Complement Factors and Cytokines
• Webinar: Development of a Cell-based Assay for Dual Purposes

With decades of experience formulating and manufacturing highly potent APIs (HPAPIs), our experts have helped sponsors move their HPAPIs from development to market, quickly and safely.

Our FDA-registered cGMP facility is equipped with Grade C and D manufacturing areas to handle highly toxic drug compounds, and on-site laboratories for all your analytical needs, including ICH stability testing, method development, and validation.

Watch our experts in action as they scale up your projects using various techniques and dosage forms, from prototype formulation to commercial scale batches.

Do you have an HPAPI in your pipeline that needs to be developed and manufactured? Get in touch today.

Related Resources:

• Webpage: Full-Service Contract Manufacturing and Analytical Services
• Interview: How We Successfully Handle and Manufacture Your HPAPIs and Controlled Substances
• Podcast: Altasciences’ Experts Talk High Potency Manufacturing Solutions

Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining drug development solutions, whether for a single study or multiple programs, to offer an integrated/synchronized approach to CRO and CDMO services from lead candidate selection to clinical proof of concept, and beyond.

Imagine a CRO/CDMO that can streamline your drug development from lead candidate selection to clinical proof of concept. Altasciences can proactively plan your clinical program while your preclinical safety assessment is ongoing. From preclinical to clinical, we can reduce the timeline of your early phase drug development program by up to 40%.

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Speak with our experts to discuss your drug development needs.

You may also be interested in the following

• Webpages:
  • Proactive Drug Development
  • Clinical Research Services
  • Preclinical Services
• Playbook: Real-World Insights From Biopharma Dive’s Survey With Industry Executives

Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining drug development solutions, whether for a single study or multiple programs, to offer an integrated/synchronized approach to CRO and CDMO services.