Javascript must be enabled for the correct page display
Skip to Content
navigation opener
Events

Contract Pharma’s 25th Annual Contracting & Outsourcing Conference

Bora Biologics will be exhibiting at Contract Pharma’s 25th Annual Contracting & Outsourcing Conference in New Brunswick, New Jersey, September 24–25.

Visit us at Booth 14 to discuss how Bora Biologics can support your biologics development and manufacturing strategy — from early technical planning through clinical and commercial supply.

As biologics programs face increasing pressure to move quickly while managing supply chain, quality, regulatory, and tech transfer risk, choosing the right CDMO partner matters. Bora Biologics brings mammalian and microbial expertise, U.S.-based GMP biologics manufacturing, and experienced technical teams focused on helping customers advance with confidence.

Let’s Talk About Your Program
Meet with our team to discuss:

  • Biologics development and manufacturing strategy
  • Mammalian and microbial manufacturing capabilities
  • Tech transfer planning and execution
  • Clinical and commercial supply readiness
  • Quality, inspection, and regulatory considerations
  • Risk reduction across development and manufacturing

Whether you are preparing for a key development milestone, evaluating CDMO options, or planning for future commercial supply, we welcome the opportunity to connect.

Schedule a Meeting
Planning to attend Contract Pharma 2026?  Schedule time with Bora Biologics in advance to discuss your biologics program and manufacturing needs.

✅ Request received. We will connect with you shortly to schedule a meeting.







    Filter

    Bora Biologics

    the logical choice

    Join the ranks of biopharma pioneers who trust us.
    Explore how we minimize risks and accelerate your success.

    Partner with us

    Client-Centric

    100% commitment to supporting your success

    We have been the client, bringing multiple biologics from IND to BLA. Your needs and goals are at the forefront of our approach. By involving you in every step of the process, we ensure transparency and alignment, reducing the likelihood of misunderstandings and ensuring the outcome meets your expectations.

    Experience

    15+ years developing & manufacturing biologics

    We have honed our ability to navigate complexities. Our track record from concept to commercialization means we can apply best practices and lessons learned, ensuring smoother project execution.

    Expertise

    Over 200 seasoned scientists & regulatory professionals

    Our team exudes deep knowledge and specialized skills. This expertise allows us to foresee potential challenges and implement proactive solutions, reducing the likelihood of setbacks.

    Commercial-Ready

    2 US FDA registered GMP manufacturing facilities

    We focus on delivering solutions that are ready for market. With clinical to commercial scale facilities consistently meeting compliance standards, we ensure your project is primed for success, minimizing the risk of costly revisions or delays.

    Allied

    access to global CDMO resources

    Our partnership with Bora Pharmaceuticals provides additional resources and insights. This network enables us to leverage shared knowledge and expertise, further mitigating risks and accelerating the overall success of your project.