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R&D Experimental CRO Services: COVID-19 Research

As the COVID-19 pandemic arrived in 2020, there was a limited set of biological tools already developed to perform research on SARS-CoV-2. The previous outbreak of SARS-CoV-1 in 2002 until 2004 wore off by itself, and at the time some antiviral projects and vaccine development had started. However, all projects finally stopped, and very limited R&D tools such as cell lines or animal models were optimized for research on the coronavirus.

In 2020, with the apparition of the new coronavirus SARS-CoV-2 and the worldwide pandemic of COVID-19, R&D service companies and research laboratories started to use existing research models and tools adapted to SARS-CoV-2 and create new ones: in vitro assays, ex vivo assays, in vivo tests on infectable animals for the development of COVID-19 drugs, vaccines, validation of immunological, PCR or side-flow diagnostic kits, measurement of virucidal effects of materials directly on SARS-CoV-2.

Finding the right service laboratory with the set of competencies required for a COVID-19 project, however, has been proven to be difficult.

This is why Labtoo developed a tailor-made service to support Labs, Biotechs, Medtech, and Pharma companies in their SARS-CoV-2 research programs.

Labtoo can look for any type of SARS-CoV-2 experimental services,  for the development of new drugs and the development of diagnostics assays. We work with a large international network of laboratories and service companies to provide the largest options for your project.

Our Experimental Services for SARS-CoV-2

 

We are specialized in tailor-made projects for the pharmaceutical and biotech industry.

Select your options and start building your project.

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COVID-19 DRUG DEVELOPMENT

A full set of services to get started with COVID-19 new drug development.

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COVID-19 DIAGNOSTICS ASSAY DEVELOPMENT

In vitro services to validate diagnostics assays for SARS-CoV-2 in comparativee and efficacy studies.

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COVID-19 VACCINE DEVELOPMENT

In vitro services to validate diagnostics assays for SARS-CoV-2 in comparativee and efficacy studies.

What is included in our services?

Our team will handle your R&D service management from the beginning to the end

Perform a feasibility study by looking for existing expertise available within the network of partners

Set up a study protocole, financial quotation and preparing contracts with lab partners

Implement the study plan into a schedule, collect all needed materials and reagents and execute the service

Do you need more information about our experimental services?

How are the service providers selected?

 
At Labtoo, we have built a network of 500 service providers from academia, hospitals and private companies. 
 
We are very closely with our customers to understand exactly what is needed: is it a strong expertise on a scientific domain, or a technological requirement, or a little bit of both.
 
We have developed a unique method to qualify and select the best partner for each project
 
During the feasibility study that we carry out with our customers, we will ask a series of questions that will allow us to move forward in full confidence.
 

Selecting the right structure type

When looking for a CRO, there are several choices: generalist or specialized CRO, small or large structure, well-known or not... While a large CRO recognized internationally instills confidence and allows more flexibility, small and medium-sized CROs in France or Europe offer a tailor-made and highly specialized service (cancerology, neurology, cardiology, etc.) that may be more relevant to your project. Moreover, size and quality are not always correlated. 

Defining a budget 

Even if a low price is an important criterion, it should not be the major one. If a services provider seems more relevant and more competent, although more expensive, it may be worthwhile to concede to a more substantial investment, which may protect further from additional costs (due to deadlines issues, or even a change of services provider during the study).

Rely on trust... or on a previous experience!

Delays in the preclinical phases can be extremely damaging to small structures and may even jeopardize their survival. Therefore, all R&D providers must be considered trustworthy partners. When presenting the project, he must be critical of the provided elements and challenge the protocol that you are submitting to him. Good advice will save time and thus money, and a realistic time frame and a presentation of the risks involved are must-haves. And of course, getting insights from a preliminary experience is likely to help to choose.

Experience, certifications, and regulatory compliance

Depending on the stage of the project, certifications and compliance with processes might be required. It is mandatory to acquire good practices as soon as possible in the drug development process.
 
 
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COVID-19 Services
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Biological Samples
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Experimental Services
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