Excellence in Solid Oral Dosage Form Manufacturing

Ritsa Pharma Pvt. Ltd. - Your trusted partner for high-quality tablet and capsule manufacturing. Specializing in solid oral dosage forms with state-of-the-art facilities and uncompromising quality standards.

Pharmaceutical Research
Innovative Research
Advanced Technology
Laboratory
ABOUT RITSA PHARMA

Pioneering Pharmaceutical Excellence Since 2020

Ritsa Pharma is a contract manufacturing organisation that provides state of the art manufacturing services to Pharmaceutical companies.

Our state-of-the-art infrastructure and equipment meets current global regulatory requirements, to manufacture quality solid oral drug products. Our services are tailer made to offer small to low scale manufacturing of finished pharmaceutical products to market and clinical supplies. We support our partners with all their associated manufacturing, analytical and packaging needs such as analytical method validation, clinical packaging etc.

Incorporated in 2020, Ritsa Pharma with a unique business model, scientific expertise across new therapeutic modalities, an experienced management team, and an independent Board committee, Ritsa Pharma works for clients around the globe, delivering services that benefits human. As a strategic partner to its clients, often working as an extension of their internal teams, Ritsa Pharma offers innovative, flexible, and efficient approaches to scale up rapidly. This, in turn, enables faster go-to-market and access to patients.

Ritsa Pharma Pvt. Ltd. is located in Neovantage Innovation Park, Building: 1800, Genome Valley, Hyderabad, India

WHY CHOOSE RITSA PHARMA

Comprehensive Pharmaceutical Solutions

From concept to market, we provide end-to-end pharmaceutical services

OUR VISION

To be one of the Reliable Contract Manufacturing Organization for Finished Pharmaceutical Products acting with Integrity, building Trust in the customer services focusing on Specialty products to deliver Ambitious goals of the business.

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OUR MISSION

To provide best-in-class development & manufacturing services to the customers by meeting stringent regulatory and risk management requirements for ensuring Quality and Compliance in the products delivered at competitive costs.

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OUR PURPOSE

To Employ right People, Use Efficient Processes to bring out Effective Products of customers’ need.

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Research Laboratory
OUR VALUES

Championing Integrity, Inspiring Operational Excellence

Integrity and excellence are the cornerstones of everything we do at Ritsa.

Integrity

To be ethical, honest and transparent in all we do

Excellence

To commit ourselves to the highest levels of operational excellence

OUR COMMITMENT

Driving Pharma Solutions with Purpose and Precision

At Ritsa, we aim to uphold highest standard of manufacturing excellence using our skills, technology and experience to find solutions to the customer’s most complex challenges.

Customer

Deliver manufacturing innovation that meets our clients' requirements and, in turn, helps them to meet the needs of the people and patients they serve

Employees

Provide a safe work environment. Offer personal development in scientific, managerial and leadership skills to foster professional growth

Society & Environment

Safeguard the environment by reducing our environmental footprint and producing safe products and supporting the community around us

Research Laboratory
OUR JOURNEY

Milestones & Achievements

Tracking our significant milestones since inception.

2020

Inception

Company established with a vision for excellence.

2021

Site Development

State-of-the-art facility built at Genome Valley, Hyderabad.

2023

FDA Inspection

Successfully cleared FDA regulatory compliance inspection.

2024

Commercial Operations

First batch of products dispatched successfully.

2025

FDA Inspection

Successfully cleared FDA regulatory compliance inspection.

KEY PEOPLE

Management Team & Directors

Meet the leaders driving innovation and excellence at Ritsa Pharma

Our Services

Comprehensive Pharmaceutical Solutions

From concept to market, we provide end-to-end pharmaceutical services

Manufacturing

From pilot-scale bioequivalence (BE) manufacturing and reliable clinical-supply provision to robust registration-stability support and seamless commercial-scale production, our pharmaceutical services ensure your program advances smoothly at every stage.

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Analytical

Our analytical services span rigorous method validation and verification, comprehensive release testing, and thorough stability studies—ensuring data integrity and regulatory compliance at every stage.

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Clinical Packaging

Our clinical-packaging solutions include precise single-blind packaging for unbiased patient dosing and secure double-blind packaging to maintain study integrity—ensuring consistency, confidentiality, and compliance throughout your trial.

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OUR CORE CAPABILITIES

Advanced Technologies Driving Innovation

Cutting-edge expertise and technologies that set us apart

Wet Granulation

High-shear mixing, top-spray granulation, and pilot-scale bottom-spray granulation for uniform, scalable formulations.

Dry Granulation

Chilsonator compaction for precise pre-compression and densification of powder blends.

Blending and Lubrication

Efficient blending and lubrication using 30–150 L cone blenders and 150–600 L V blenders

Tableting

Monolayer and bilayer tableting for versatile dosage form development.

Capsule Filling

Precise empty hard gelatin capsule filling.

Tablet Coating

Tablet coating with equipment capacities from 2 to 56 L.

Bottle Packaging

Fully integrated bottle packaging line offering automated capping, labeling, and sealing for streamlined, compliant operations.

Blister Packaging

High-speed, precision blister packaging solutions ensuring product integrity and regulatory compliance.

Quality Control
Quality & Compliance

Ritsa prioritizes quality over profits

We strongly believe and emphasize on the phase and business model appropriate quality management system (QMS), meeting the essential regulatory requirement. Our QMS focuses on continual improvements by adopting technological advances and keeping in line with various regulatory requirements.

GMP as per schedule–M of Drugs and Cosmetics Act (India)
ICH series guidelines
EU-GMP
21 CFR parts 11, 210, 211
New drugs and clinical trials rules, 2019
Learn More About Our Quality
Address

Building 1800, Neovantage Innovation Park,
Genome Valley, Hyderabad, India