

TOTELL
Biotech Consulting & Clinical Development Solutions, located in the heart of BioBeach
Go-to-Market Strategy
All of your efforts accumulate to one final stage of clinical development– commercialization. Crafting an effective Go-to-Market (GTM) strategy is a pivotal step and is about more than just launching a product; it's about positioning it strategically, identifying target markets, and devising plans to reach key stakeholders effectively.
Our seasoned professionals have successfully launched numerous types of therapeutics across a diverse range of therapeutic areas. They are well-versed in the intricacies and best practices involved in effectively bringing drugs, devices, or combination products to the market. Their expertise can position your product for success and reach the patient population who needs it most by conducting thorough market analysis and competitor research, engaging stakeholders, and designing and executing a strategy for launch and adoption into the healthcare landscape.
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Regulatory Affairs & Technical Writing
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Submissions & Applications (domestic and international)
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New Drug Application (NDA)
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Abbreviated New Drug Application (ANDA)
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Biologics License Applications (BLA)
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Technical & Medical Writing
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Technical Documents for All Modules
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Labels & Packaging
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Conference posters
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Investor presentations
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Government Agency/Health Authority Representation & Mediation
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Reviewing, Formatting, eCTD Publishing, & Submission
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Document Changes & Maintenance
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**see Regulatory Affairs in Clinical Trials section for more information
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Medical Affairs
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Post-Market Studies
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Safety & Adverse Event Reporting
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**see Medical Affairs in Clinical Trials section for more information
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Marketing & Sales
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Supply Chain Management & Logistics
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Commercialization
**see Commercialization & Post-Market section for more information
San Diego, CA info@Totellinc.com
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