PM Soft Solutions

Pharma & Chemical

Integrated Project Excellence & Digitalization for Regulated Innovation

In the highly regulated and innovation-driven Pharma & Chemical industry, project delays, disconnected systems, and inconsistent processes can derail both time-to-market and compliance. From Concept to Commercialization, organizations need a structured yet flexible approach to manage complex product pipelines, regulatory timelines, and capital investments.

That’s where PMSoft comes in—with a proven blend of Project Management Consulting and ROI-focused Digitalization built specifically for the Pharma and Chemical ecosystem.

What We Offer: Domain-Driven Project & Digital Solutions

Project Management Consulting for Pharma & Chemical

Digitalization Modules Designed for Pharma & Chem

Each module integrates compliance, traceability, and performance metrics—turning operational complexity into strategic clarity.

New Product Development (NPD)

Digitalize your Concept to Commercialization journey with structured workflows and cross-functional visibility.

Product Basket

Capture, evaluate, and evolve early-stage product ideas with a future-ready innovation repository.

Enquiry Module for CDMO

Streamline client enquiries, proposal status, and conversion tracking—digitally linking revenue potential to project execution.

Dossier Management

Centralized document workflows for ANDA, LDR, and global deficiency handling—fully audit-ready.

Project Cost & CAPEX Management

From estimation to execution, align budgets, track ROI, and avoid overspends with structured financial control.

Timesheet for R&D

Track effort, associate hours to projects, and understand manpower cost in development with digital precision.

Looking to bring structure, speed, and ROI to your Pharma or Chemical projects?

Connect with us to learn how PMSoft’s Consulting + Digitalization model delivers transformation that sticks.

Contact us at : info@pmsoft.com

Why PMSoft for Pharma & Chemical

FAQs

Questions Asked For Pharma Chemical

Do you still have any questions, let us know. We would be happy to assist.

APIs (Active Pharmaceutical Ingredients) are the main components in medicines that produce the intended effects. They are often combined with excipients to create the final drug form.

GMP (Good Manufacturing Practice) ensures that products are consistently produced and controlled according to quality standards. It is crucial in pharmaceuticals to ensure drug safety and efficacy.

Research and Development (R&D) drives innovation in drug discovery, formulation, clinical trials, and product improvement, and is critical for long-term growth and compliance.

The chemical industry supplies key intermediates, solvents, and other raw materials used in the synthesis of Active Pharmaceutical Ingredients (APIs).

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