About Us
TLR TECH supports Pharma, Biotech, Medical Devices & Diagnostic companies in simplifying & expediting the regulatory approval process of investigational products.
The key elements for expediting product development are:
- Strategic clinical development program
- Regulatory expertise of relevant regulatory authorities requirements for your specific product
- Efficient Project Management
- PROFESSIONAL MEDICAL WRITING
TLR TECH was founded by a seasoned medical writer and a CRO executive with over 13 years of in-depth global CLINICAL RESEARCH understanding. Since its foundation, TLR Tech was involved in multiple projects for over 40 different clients (large & midsize pharma, biotech, medical device, diagnostic, CRO and venture capital companies) in Asia (Israel and Singapore), US and Europe, and worked on various therapeutic indications, study phases, and products (drugs, devices, combination products, biologics, diagnostics and gene therapy).
TLR TECH PROFESSIONALS, with advanced life-science background, are familiar with relevant regulatory requirements. TLR TECH PROFESSIONALS provide coherent and easy-to-read clinical research dossiers while maintaining scientific integrity in interpreting and presenting your clinical data.
For a competitive price proposal or for FREE sample dossier template or FREE expert protocol review service
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