Bora Biologics

Bora Biologics
Bora Zhunan Production Facility

Flexible and integrated solutions for biologics development and cGMP manufacturing

From cell-line development and formulation to analytical services and commercial cGMP manufacturing, Bora now provides tailored development and manufacturing services to biologics developers end-to-end. With operations in newly acquired Taiwan facility, Bora has the capability to deliver high-yield processes and the program management needed to launch even the most challenging molecules successfully.

Bringing commercial success to our partners through broad operational expertise

The experienced biologics team are highly skilled experts at guiding biologics programs from their earliest stages, through development and on to patients as efficiently as possible.

Temperature & Humidity Controlled Warehouse
Bora Zhunan Production Facility

Flexible single-use manufacturing technologies at an advanced global site

From cell-line development and formulation to analytical services and commercial cGMP manufacturing, Bora now provides tailored development and manufacturing services to biologics developers end-to-end. With operations in newly acquired Taiwan facility, Bora has the capability to deliver high-yield processes and the program management needed to launch even the most challenging molecules successfully.

Disintegration Pharmatron

Cell Engineering - Developing protein therapeutics is difficult because they are highly complex molecules that are grown by living cells cultured and cultivated in a precise, reproducible fashion. At Bora Biologics, we have mastered the art and science of cell engineering, cell culture, and protein purification.

Fette 2200i Tablet Press

Platform – As a top CDMO, we have a platform approach to developing biologics that allows us to perform all activities needed to transform biologics from concept to commercial product in-house.

Key Features

  • Segregated USP/DSP
  • 2x 500L bioreactors
  • Gowning facilities
  • Separated post viral processing
  • Clean utility systems (WFI/CS/CA)
  • HVAC systems and controls

Facility capabilities

  • Segregated upstream and downstream processing areas
  • Segregated media buffer preparation and holding areas
  • A two-suite purification area for pre-/post-viral processing and bulk filling

Robust biologics capabilities end-to-end, designed to accommodate biopharma’s unique needs

Our end-to-end solutions for biologics include cell-line and process development, analytics and formulations development, as well as full cGMP manufacturing and drug product filling and finishing services.

Regulatory Compliance

  • cGMP, ICH, FDA, EMA, TFDA, PIC/S standards
  • Inspections and GMP Certified by TFDA
  • EU QP Passing