Welcome to

Rasal Pharma

A trusted Pharmaceutical consultant

We offer a comprehensive range of services tailored to meet your specific needs. With our expertise in complete project consultancy for pharmaceutical formulation, documentation for WHO/EU-GMP certification, GMP audit, and more, we are committed to helping you excel in this highly regulated field.

What we do

Consultancy

Complete Project Consultancy for Pharmaceutical Formulation. Our experienced team provides expert guidance throughout the entire lifecycle of your pharmaceutical formulation projects. From conceptualization to implementation and optimization, we ensure that your formulations meet the highest industry standards.

Documentation

Documentation for WHO/EU/GMP Certification. Obtaining WHO/EU-GMP certification is vital to demonstrate compliance with international regulations. Our professionals excel in preparing the necessary documentation, assisting you in achieving regulatory compliance and enhancing your credibility.

GMP Audit

Maintaining Good Manufacturing Practices (GMP) is crucial to ensure the highest quality and safety of your pharmaceutical products. Our meticulous GMP audits help you identify areas of improvement, mitigate risks, and keep your operations streamlined.

Upgradation of QMS

A strong Quality Management System (QMS) is pivotal to the success of any pharmaceutical manufacturer. We offer tailored solutions for upgrading your QMS, enabling you to meet current industry standards and regulatory requirements.

Vendor Audit

Choosing reliable vendors is key to maintaining product quality and safety. Our vendor audit services help you assess and select vendors who adhere to the necessary quality standards, ensuring a seamless supply chain for your business.

Dossier Preparation

Preparing comprehensive dossiers is essential for gaining regulatory approvals and market authorizations. Our experts are well-versed in dossier preparation and can assist you in compiling accurate and compelling documentation for successful submissions.

EasyErp - our ERP software

Main features of ERP software

Batch Manufacturing
Quality Control
Inventory Management
Regulatory Compliance
Supply Chain Management
Financial Management
Recipe and Formulation Management
Traceability and Serialization
Document Management
Customer Relationship Management (CRM)
Reporting and Analytics
Human Resources Management
Mobile Accessibility
Security and Data Protection
Integration Capabilities

Implementing a pharmaceutical ERP system that encompasses these components and features can significantly improve operational efficiency, compliance, and overall business performance for pharmaceutical manufacturers.

GMP Training Course

Good Manufacturing Practice, or GMP, is a set of quality assurance practices promoted by regulatory authorities (including the WHO and US FDA) to ensure manufacturing processes are rigorously set and monitored. This training is designed to help you implement in an organization the increasing legislation and guidance on goods within the manufacturing industry.

What peoples say about us

"I am thoroughly impressed with the exceptional service provided by your team. From the insightful guidance on regulatory compliance to the meticulous attention given to our manufacturing processes, Rasal Pharma has proven to be an invaluable partner. "

Rajeev Lila

Managing Director, La Sante

"Rasal Pharma's team exhibits a remarkable level of expertise and proficiency in the pharmaceutical consultancy field. Their in-depth understanding of regulatory frameworks and commitment to ensuring compliance has greatly benefited our company."

Mahaveer Chachan

MD, G. D. Laboratories

"The strategic insight and unwavering support offered by Rasal Pharma have been instrumental in navigating the complex pharmaceutical landscape. Their ability to develop a tailored regulatory strategy, coupled with ongoing support, has significantly streamlined our international compliance efforts."

Sauabh Gupta

MD, Jocund India