Combining Trial Conduct and Bioanalysis for Success

Combining Phase I trial conduct of biologics and bioanalysis is critical for successful drug development. Clinical development relies heavily on bioanalytical experts to generate critical data to understand pharmacokinetics and pharmacodynamics. 

Here are just some of the benefits of working with Altasciences:

• Timed interim sample analysis for dose escalation decisions
• Rapid turnaround of PK/PD analysis between cohorts 
• Biomarker development and validation for exploratory or primary endpoints
• Proximity flow cytometry 
• Centralized scheduling between clinic and lab
• Ability to easily switch or combine platforms which are sensitive, have high throughput, and demonstrate exquisite specificity

Watch this complimentary webinar to see how you can overcome challenges throughout all phases of drug development.

Watch webinar

Have 5 minutes? Take a look at these:

• How Is Partnering with Altasciences for Your First-in-Human Clinical Trials Different?
• Microsampling in Drug Development
• Validated Bioanalytical Assay List

Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining 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.

Over 80% of drugs will fail during clinical development due to formulation challenges. Having developed, tested, and manufactured almost every type of dosage form on the market, Altasciences has the expertise to customize our services to your API’s needs, taking it through its entire lifecycle and ensuring its successful delivery ― from prototype formulation development, to scale-up and ICH stability, to clinical manufacturing and commercial supply.

Our scientists tailor your drug compound to ensure optimal solubility and bioavailability. In addition, we have extensive experience handling complex and highly potent products. Finally, our state-of the art technology and banding equipment make us leaders in the development of hard-shell, liquid-filled capsules ― a dosage form often required for poorly soluble, highly potent or low dose APIs.

Partner with us today to reduce your development timelines and risk of product failure.

You may also be interested in the following: 

• Scientific Journal: Maximizing drug formulations for first-in-human trials
• E-Book: Benefits of Liquid-Filled Capsules for Pharmaceutical Development
• Webpage: Altasciences’ Pharmaceutical Contract Manufacturing and Analytical Services
   

Sample Management Based on Your Specific Needs

Did you know that Altasciences’ Material Management Team has over 25 years of experience? Indeed, our experts in sample management processes have been supporting clinical trials worldwide for over two decades. 

We have designed an efficient system for accurate and safe clinical sample preparation, collection, and shipment from trial sites to bioanalytical laboratories. 

Watch to learn more.

Questions about our customized offering? Send us a message. 

You may also be interested in:

• Clinical Sample Collection Kits Capabilities
• Bioanalytical Services
• Clinical Services

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.

Multi-Site Clinical Trial Management and Monitoring

With extensive expertise in a wide range of study types and therapeutic areas, Altasciences’ clinical monitoring and site management teams deliver reliable data, fast. Our experts work closely with you and your sites, to guide you through the complex steps of drug development.

Clinical Monitoring:

Highly skilled clinical research associates oversee all aspects of your clinical trial conduct to ensure data integrity, patient safety, protocol compliance, and GCP.

Site Management:

Experienced project managers oversee the conduct of multi-site programs in close collaboration with key internal and external stakeholders, ensuring seamless and timely communication.

Whether as stand-alone or part of an integrated program, let’s discuss your clinical monitoring and site management requirements today.

Speak with an expert

Have 5 minutes? You may be interested in:

• Impaired Renal and Hepatic Function Trials Capabilities
• Full-Time Equivalent Capabilities
• Research Support Services Capabilities
• Integrated Drug Development Services

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.

Our Commitment to You

Your new drug could be the one that changes someone’s life. As investors in life sciences, we know that each project matters. Whether you place one study or multiple programs with us, we treat each project with the equal care and dedication it deserves, no matter the size or spend. 

We are committed to making your project a success. After all, your success is our success. And our success, together, means getting better drugs to people who need them, faster.

Speak with an Altasciences expert today. 

TAKE FIVE:

• Watch this video to experience the difference
• Check out our new interactive brochure
• Discover our Proactive Drug Development approach
• Read this blog article: Five Ways Altasciences Simplifies the Drug Development Process for You
• Catch up on our top scientific resources of 2021

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.