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BD PartnerPath™

BD PartnerPath™ Program aims to support pharmaceutical organizations that value speed to market in combination product development.2

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Customer Benefits

The BD PartnerPath™ Program aims to help anticipate obstacles, mitigate risks and solve operational challenges for customers during combination product development.

Through our program, you will gain access to low quantities* of individually available products and preconfigured product sets along with the proactive delivery of supporting documentation to help streamline device selection, inform development efforts, and help de-risk device-related aspects of the development process. 2,4

COMBINATION PRODUCT LAUNCH

Developing a combination product can be difficult. You may encounter many challenges that can delay development and launch. Ultimately, these delays increase costs, negatively impacting profitability and can decrease viability of market launch.2 Common challenges include:

  • secondary device

    Primary and secondary device identification

  • Compatability

    Drug Compatibility

  • system integration

    System Integration

  • operational

    Operational feasibility

  • testing

    Testing feasibility

  • regulatory registration

    Regulatory registration

CUSTOMER SERVICES

For complex and novel drugs, you need greater precision from the devices you choose. Primary containers, components and secondary devices should work together without impacting drug makeup and the ability to safely and effectively inject your drug.2 BD has the experience and expertise to help you efficiently select combination solutions to de-risk device related aspects of the development process.1 Our BD PartnerPath™ Program aims to support device related aspects of your drug’s development, helping to ensure you meet your drug’s launch timeliness and performance targets.

 EXPERTISE

ROBUST DATA SETS. INTEGRATED DEVICE SOLUTIONS. EXCEPTIONAL BD EXPERTISE

With the BD PartnerPath™  Program, you now have access to small-scale quantities of the primary and secondary delivery solutions to meet your needs for clinical development—along with supporting documentation and extensive BD expertise in managing system interfaces.1,3,4

So your drug gets to market as quickly as possible—and performs under real-life conditions.

Gain timely access to small quantities* of commercially available solutions for use in combination products- from early development through assembly validation.

*minimum purchase quantity at the lowest sterilized package configuration e.g. syringe tub or plunger stopper bag

Available as individual products or preconfigured product sets, our solutions can help streamline the device selection process and promote assurance in the combination of device components*.1

* The BD PartnerPath™ Program is currently available in North America, Europe, and certain regions of Greater Asia.

We can help you streamline device related aspects of your development and registration activities by proactively providing supporting documentation.4

Our expertise can enhance device related aspects of your combination product’s development. Our experience enables BD to help trouble shoot combination product development issues and recommend preconfigured product sets to meet your unique needs.1,3,4

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Reference
  1. Syringes manufactured per year > 2.3 billion – BD Internal systems (SAP ECC, SAP Legacy, Tracis, Nodum) – January 2018
  2. Market Research “Challenges with System Integration" [external study], Franklin Lakes, NJ, USA: GLG 2019
  3. BD PartnerPath™ products and packages, [Internal product list], Franklin Lakes, NJ, USA: Becton Dickinson and Company; 2020
  4. BD ERDs and Technical Documentation packages: Examples (Ex: STMT-QE20183091-Selflife statement PR, TDS20191489 rev 6-Appendix of TDS20181495-Plunger Rods,TDS20181495 rev 05 Plunger Rods/ADF122 rev2_47404808_fullpackage)