BioPharma Connections

BioPharma Connections

Business Consulting and Services

Reno-Tahoe, Nevada 555 followers

Bringing People and Ideas Together for the Advancement of Life Sciences™

About us

Helping to Bring People and Ideas Together for the Advancement of Life Sciences Founded in 2007, BioPharma Connections (formerly Business Development Connections) is an independent, woman-owned, San Francisco-based biopharmaceutical consulting company that provides strategic business development support to life sciences companies, CROs, CDMOs, technical engineering/facilities service providers & life sciences consulting firms. We consult with our clients in pharmaceutical, biotechnology, medical device, and diagnostic companies to identify outsourcing, partnering, or investment needs from concept to commercialization. BioPharma Connections offers you the facilitation of quality connections, relationship management, follow-up and business development support.

Industry
Business Consulting and Services
Company size
11-50 employees
Headquarters
Reno-Tahoe, Nevada
Type
Self-Owned
Founded
2007
Specialties
Pharmaceutical Development, Biotechnology Development, Life Sciences Business Development, Quality Compliance and Regulatory, Life Sciences Facilities Support, Biotechnology Business Development, Pharmaceutical Business Development, Clinical Support, Licensing Support, and Biopharmaceutical Consulting

Locations

Employees at BioPharma Connections

Updates

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    555 followers

    Let's meet at the Hanson Wade Derm Summit in Boston from November 11th to 14! We'd love to schedule a meeting to discuss your current interests in product development, manufacturing, or licensing. Message us to set up meetings with Genemarkers and/or CPL. Genemarkers provides preclinical and clinical research services, with expertise in dermal cell biology and genomics-based technologies. CPL has over 33 years of experience in providing product development and CDMO support for liquids and semi-solids with an excellent regulatory compliance history with the FDA and Health Canada. #dermatologydrugdevelopment #hansonwade #dermatology #boston

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    Please don’t miss this opportunity today to learn about the “Essential Rules for IRT In Clinical Trials” presented by Craig Mooney, Global Head of IRT at Taikun Pharma at 9 am Pacific! Please be sure to register using the link below if you would like to attend.

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    Join Craig Mooney from Taikun Pharma Services on Thursday, October 24th at 9 am Pacific for a live webinar! Join industry expert Craig Mooney for an interactive session and learn his 11 Commandments for Interactive Response Technology (IRT) systems. Some are crystal clear, while others challenge the status quo and rethink traditional practices. These 11 commandments come from Craig’s extensive 30-year journey as a vendor, business owner, and sponsor.

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    Join LGM Pharma on October 17th for an insightful webinar focused on addressing the key challenges faced by Quality Control (QC) laboratories. From keeping up with evolving regulations and mitigating supply chain disruptions to improving communication and maintaining equipment, QC labs play a critical role in ensuring product safety and precision. During the discussion, experts, Shailesh Vengurlekar and Diem Hoang will cover practical strategies for regulatory compliance, enhancing communication within and outside the lab, equipment maintenance, and talent retention. Gain valuable insights and actionable solutions to maintain operational excellence in your QC processes. Don’t miss this opportunity, register today! Click here to register: https://lnkd.in/g3qBYF8n

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    Join Craig Mooney from Taikun Pharma Services on Thursday, October 24th at 9 am Pacific for a live webinar! Join industry expert Craig Mooney for an interactive session and learn his 11 Commandments for Interactive Response Technology (IRT) systems. Some are crystal clear, while others challenge the status quo and rethink traditional practices. These 11 commandments come from Craig’s extensive 30-year journey as a vendor, business owner, and sponsor.

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    I’m looking forward to attending the Boyd’s’ webinar in September to learn more about how to de-risk a clinical development plan. Please see a summary below and I hope that you can all join us!!

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    The clinical development process can be tricky but Boyds has tips and expert advice on de-risking your clinical development plan. Join our Complimentary Webinar on Thursday, June 27th at 9 am Pacific to learn more from Boyds' experts Dr. Karen Mullen and Dr. Harriet Gray Stephens as they take us through essential strategies and insights to navigate and mitigate risks in your clinical development process. Register here: https://lnkd.in/ggWQZ-_i #clinicaldevelopment #clinicaltrials #drugdevelopment #Boyds #webinar #freewebinar

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    Meet Boyds in person near you! Boyds will be attending several conferences between September 11th and October 4th. If you're attending any of these conferences, Boyds welcomes the opportunity to meet and discuss your needs for regulatory, product development, program management, and clinical and medical support. See more details in the event post!

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    Meet with LGM Pharma’s Director of API Sourcing, Alberto Santana, at ChemOutsourcing in Parisppany, NJ from September 3rd to 6th. LGM is known for their client commitment and smooth API sourcing, as they have delivered over 6,000 APIs directly to their clients doorsteps in the past three years. If you are interested in meeting with LGM Pharma at the conference please email Mya Jackson mjackson@biopharmaconnections.com #APISourcing #ChemOutsourcing #LGMPharma

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    Join our Complimentary Webinar on Wednesday, September 11th at 9 am Pacific to learn more from Smaranda Doucet, CEO of FlowTrial, as she explains how expert sponsor oversight can enhance your clinical trials. By the end of this session, you'll have actionable insights to enhance your oversight capabilities and a clear roadmap to reach your oversight goals. Register here: https://lnkd.in/guWpyFAq #ClinicalTrials #ClinicalTrialOversight #SponsorOversight

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    New Date for Boyds Webinar: How To De-Risk Your Clinical Development Plan. Register now and mark your calendars for Thursday, September 26th at 9 am PDT! Dr. Karen Mullen and Dr. Harriet Gray Stephens will take us through essential strategies and insights to navigate and mitigate risks in your clinical development process. Register here: https://lnkd.in/ggWQZ-_i

    View organization page for BioPharma Connections, graphic

    555 followers

    The clinical development process can be tricky but Boyds has tips and expert advice on de-risking your clinical development plan. Join our Complimentary Webinar on Thursday, June 27th at 9 am Pacific to learn more from Boyds' experts Dr. Karen Mullen and Dr. Harriet Gray Stephens as they take us through essential strategies and insights to navigate and mitigate risks in your clinical development process. Register here: https://lnkd.in/ggWQZ-_i #clinicaldevelopment #clinicaltrials #drugdevelopment #Boyds #webinar #freewebinar

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