Industries

Biologicals

Biologicals

Ficus Realtime offers specialized support in the development, qualification, and regulatory compliance of biological products—including vaccines, monoclonal antibodies, biosimilars, recombinant proteins, blood products, and cell & gene therapies

Biologicals are highly complex and sensitive, requiring precise handling, validated manufacturing processes, and strict regulatory oversight. We work closely with your team to ensure quality, safety, and compliance from R&D to commercial launch.

Our Services Include:
Biologics Regulatory Strategy:
Regulatory pathway selection: IND, BLA, biosimilars
Dossier preparation in CTD/eCTD format
Global compliance: FDA (CBER), EMA, CDSCO, WHO, ICH
Quality Systems & GMP Compliance:
Design and implementation of biologics-specific QMS
Process validation: upstream (cell culture), downstream (purification)
Cleaning validation, aseptic process validation
Facility qualification (HVAC, cold storage, biosafety levels)
Analytical & Stability Support:
Analytical method development and validation (ELISA, bioassays, etc.) ICH-compliant stability testing for biologics Cold chain validation and packaging qualification Documentation & Audit Readiness:
Batch manufacturing records and quality documentation Risk assessments, deviation investigations, and CAPA support Pre-approval inspection (PAI) and regulatory audit preparedness

 

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