Sign Up for Free Office Hours
You guide the discussion.
We provide expert insights.
Address challenges in clinical development, regulatory compliance, and patient engagement with an expert. TransPerfect Life Sciences offers a unique opportunity for free consulting through office hours with our subject matter experts. Explore some of your most pressing questions, without the cost or sales pitch.
Sign Up Today
What to Expect During Free Office Hours
Our experienced professionals offer tailored advice and solutions based on your most pressing challenges. Guide the conversation, and get real-time feedback. Expert insights will help you build better informed strategies.
Request a one-on-one meeting with an expert
Attend your 15-30 minute session (at no cost, without a sales pitch)
Get free insight
Are Free Office Hours Right for You?
If you are in a senior leadership position looking for some more insight without spending money or engaging in direct sales conversations, this is a great way to explore some of your most pressing questions. Our free office hours provide insights for all content, language, and data needs throughout the entire pharmaceutical development process, from lab to launch and from patient to practitioner.
Popular COA topics:
- Licensing Copyrighted Instruments
- Selection of Instruments
- Translation & Linguistic Validation Processes
- Cognitive Debriefing
- eCOA supplier selection
- eCOA language implementation process
- COA/eCOA Timelines
- COA Libraries
Popular Medical Writing Topics:
- Informed consent forms
- Clinical trial disclosure (plain language/lay summaries)
- Patient and HCP advocacy
- Publication and dissemination
- Training and elearning
- Literature monitoring
- Quality
- Regulatory submissions
- Language, culture, and accessibility considerations
Popular AI/ML Topics:
- Unstructured data set annotation
- Machine translation of mass content
- GenAI reports for real-world evidence monitoring
- Medical Writing, Clinical Trial Disclosure, and Lay Summaries
- EU CTR operational impacts on authoring and submission activities
- Redaction (clinical trial applications, results, clinical study reports)
- Translation / localization (process optimization, integration)
- Safety intake and translation for triage
- Medical info intake and query translation (public/patient/HCP to sponsor)
- Patient queries to sponsor from web, support programs
Get Free Insight: Request Office Hours with an Expert
Make better informed decisions about your clinical content workstreams with free expert insight.