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Seamless CDMO partnership across the drug product lifecycle

From GxP lab support to formulation to full-scale manufacturing, Pinnaql helps CDMOs deliver compliant, scalable, and efficient solutions for their clients.
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Scientists in lab
CDMO manufacturing process

Helping CDMOs scale with speed and compliance

As a Contract Development and Manufacturing Organization, you're under constant pressure to deliver scientific excellence, accelerate timelines, and maintain regulatory compliance across multiple clients and products. Every phase must be optimized and inspection-ready, from formulation and analytical development to scale-up and quality control.

Pinnaql partners with CDMOs to provide cross-functional engineering, lab, and compliance support tailored to your evolving portfolio. Our experts embed within your teams to streamline development, de-risk tech transfers, and build scalable systems.

How we support CDMOs

Pinnaql strengthens your position as a trusted development and manufacturing partner

01

End-to-end lifecycle support

Support from early formulation through commercial launch—including CQV, tech transfer, and process optimization.

02

Cross-functional expertise

Engineers, scientists, and QA professionals working as one team.

03

Flexible & scalable solutions

Adaptable services for growing portfolios, from pilot to commercial manufacturing.

04

Audit-ready compliance

Support for client, FDA, EMA, and third-party audits.

05

Accelerated timelines

Integrated tech transfer, validation, and risk mitigation strategies

Where we excel in CDMO operations

Drug formulation testing

Drug development & formulation

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We support your scientists and SMEs with efficient laboratory operations and compliance, including formulation, analytical development, testing, and lifecycle management.
HPLC, GC, MS, FTIR, UV-Vis systems
Dissolution, particle sizing, and pH analysis equipment
Method development, validation, and lifecycle management
Sterile drug filling

Manufacturing & scale-Up

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We help CDMOs scale efficiently from pilot to commercial production with minimal risk.
Pilot-scale reactors, bioreactors, and filtration systems
Chromatography columns (affinity, ion exchange)
Mixing and blending equipment, process control systems (SCADA/DCS)
Fill/Finish and packaging lines
Analytical method development

Quality control & compliance (GMP, CQV)

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Pinnaql ensures your labs and facilities meet evolving GMP standards and remain inspection-ready.
Environmental monitoring and cleanroom control
CQV protocols, temperature mapping, and water system validation
CSV tools, GMP documentation, and deviation response systems
Laboratory and manufacturing systems, master validation plans, and CQV services

Our services

Explore our cross-functional solutions that support our CDMO partners
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Manufacturing technical operations

Engineering, scale-up, program management
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Quality systems & lifecycle solutions

QMS development, eQMS, regulatory response
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Quality operations & assurance

SOPs, CAPA, CQV, CSV
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Lab tech operations & lifecycle services

Asset onboarding, validation, lab compliance
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Automation, AI & digital transformation

Process automation, predictive monitoring
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Let’s accelerate your clients’ path to market

Partner with Pinnaql to expand your CDMO capabilities with scalable, compliant, and technically sound solutions—built for every stage of the drug product lifecycle.

Visit us

101 Lindenwood Drive, Suite 225, Malvern, PA 19355

Visit us

9800 Crosspoint Blvd, Suite 200, Indianapolis, IN 46256

Get in touch

(484) 321-3339