Bringing Clarity to the Complexity
Communicating with patients, regulators, and investigators, medical writing requires you don’t miss out on any of the details. From early-phase protocols and Investigator’s Brochures (IBs) to patient-facing Informed Consent Forms (ICFs), and from ongoing study materials to the final Clinical Study Reports (CSRs) and regulatory submission dossiers, complex data and details need to be translated into clear, well-structured documents. LabConnect excels in working with your cross-functional teams to gather up-to-date information and incorporate feedback while adhering to stringent guidelines and timelines.
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Niche Specialized
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Pre Clinical and
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Our Medical Writing Capabilities
It’s more than knowing documents, it’s knowing a language. A well-written protocol can prevent operational errors, and a well-crafted CSR and submission can smooth the path to regulatory approval. LabConnect can provide a Medical Writer to meet your requirements in expertise and therapeutic area focus to ‘speak the language’ of that study or indication.
Some of our LabConnect capabilities include:
- Protocol development
- Investigator’s brochure (IB)
- Informed consent forms (ICF)
- Clinical study reports (CSR)
- Regulatory submissions
- Safety reports & narratives
- Publications & communication
- Quality control
15yr 
History of Regulated Bioanalytics
200 + 
Drug Products Managed
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Request a quote from our dedicated team by filling out the form today.
