Svar Life Science

June 1, 2023

The Importance of Timing and CRO Expertise in Drug Development

On Tuesday, May 31, 2023, we had the pleasure of participating in a Good Morning meeting seminar hosted by Medicon Valley Alliance on the importance of timing and CRO expertise in drug development. The seminar was attended by professionals from the pharmaceutical industry, and it was an excellent opportunity for us to share our offer and expertise with the attendees. 

In this blog post, you can read the key takeaways from the seminar and how working with a specialized CRO like Svar CRO can benefit your drug development.

June 1, 2023

The Importance of Timing and CRO Expertise in Drug Development

On Tuesday, May 31, 2023, we had the pleasure of participating in a Good Morning meeting seminar hosted by Medicon Valley Alliance on the importance of timing and CRO expertise in drug development. The seminar was attended by professionals from the pharmaceutical industry, and it was an excellent opportunity for us to share our offer and expertise with the attendees. 

In this blog post, you can read the key takeaways from the seminar and how working with a specialized CRO like Svar CRO can benefit your drug development.

Insights from regulatory expert

During the seminar,  Marianne Scheel Fjording, a regulatory expert, presented how to prepare a request for proposal and key points to consider when outsourcing bioanalytical work packages. She highlighted the benefits of working with a specialized CRO like Svar CRO, such as access to regulatory knowledge, specialized expertise, lab capacity, flexibility, project management, and innovation.

We also discussed the relevance of key analysis of the concept of use in drug development, emphasizing the need for well-planned and executed fit-for-purpose immunoassays.

These assays are critical in determining the safety, efficacy, and pharmacokinetic properties of a drug candidate. 

 

Svar CRO, your local, specialized partner!

One of the key takeaways from the seminar was the importance of applying the right level of compliance and understanding the scientific context. At Svar CRO we believe that right collaboration is key to drug development.  As a CRO, we can offer our clients a range of services, including assay development, validation, sample analysis, data management, and regulatory support.

  • Svar CRO Services operates in a regulated environment where all studies are performed using validated equipment.
  • Svar CRO Services expertise secures a cost and time-effective process combined with the right level of compliance and science.

We had a great time at the breakfast seminar, and we hope that the attendees found it informative and engaging.  As a specialized CRO in the Swedish-Danish Life Science ecosystem, we look forward to future partnerships and collaborations with the pharmaceutical industry, and we invite you to contact us to learn more about our services.

Let’s develop the future of Danish & Swedish life science together!

 

 

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About Svar CRO Services

Our range of CRO services for biologics and biosimilars includes Bioanalytical Services (GCP, GLP), QC Testing services (GMP), and Biomarker Discovery Services.

Benefit from our experience in multiple regulatory frameworks applications & drug modalities:

  • PK/TK/PD Assay Development and Validation
  • PK/TK/PD Assessments
  • ADA and NAbassays Optimization and Validation
  • Immunogenicity Assessments (ADA and NAb)
  • Biomarker Assay Development and Validation
  • Customized Method Development and Validation
  • Commercial kit validation for Biomarker Assays
  • Exploratory Potency using Cell-based Assays
  • GMP Cell-based Potency Assays

Our services help ensure that your product meets all the necessary requirements for safe and effective use.

Contact us today to talk about your CRO needs.

Talk to our experts now!