Our Services
TLR Tech is happy to provide a FREE expert review of your clinical study protocol to ensure ICH-GCP compliance.
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TLR TECH Clinical Research Professionals are expert in
- Medical Writing
- Clinical study protocols
- Clinical study reports
- Clinical sections of IND, CTD/NDA, IDE, 510k and PMA
- Investigator's Brochures
- Annual Safety Reports
- Risk Management Plans
- Safety narratives
- Literature search & review
- Patient information leaflets
- Study newsletters
- Educational and training documents
- Strategic and Regulatory Consultation in collaboration with US Regulatory Experts
- Project Management
- Overall study coordination & documentation
- Study design
- Study logistics
- Study start up, ongoing and close out activities
TLR TECH fully complies with international regulatory requirements (such as ICH E6 and E3 guidelines, ISO 14155 part 1 & 2, FDA CFR, EMEA, MDD).
TLR Tech's Clinical Research Professionals have advance life-science degree, experience in most therapeutic areas and worked extensively in the following fields:
- Central Nervous System
- Anti-infectious Diseases
- Endocrinology
- Oncology
- Cardiovascular
- Dermatology
- Respiratory
TLR TECH also works closely with highly experienced clinical monitors and collaborates with US and European regulatory experts to provide its customers a broader range of clinical and regulatory consulting services.We would be happy to refer you to these consultants as a courtesy service.
For a competitive price proposal
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