Ours is a professionally managed firm, involved in providing consultancy services for pharmaceutical plant installation requirements. We are based in Delhi, India and serving clients in the surrounding regions. Backed by a pool of qualified and skilled professionals, we are rendering solutions for small and large plant installation works. Besides, we assist clients in blueprint designing, documentation and for completing other legal procedures. The fee we charge for our services are reasonable, clients can contact us anytime through our website.

RASAL PHARMA also specifically develops and conducts in-house training courses for your company. We concentrate on an overview of the comprehensive national and international regulations as well as on relevant GMP guidances in your environment. We facilitate implementing GMP on a day-to-day basis, promote understanding for following the GMP regulations and foster a positive attitude towards GMP. Discussing current issues also makes your staff aware of GMP regulations and solves existing problems.

The following training courses are available:

• Pharmaceutical Production
• Quality Control
• Quality Assurance
• Pharmaceutical Development
• Pharmaceutical Technology
• Storage
• Administration
• Validation
• Inspection Preparation

Provide advice and answer your questions on the drug registration process.

• Prepare dossiers to support drug or device registration with different Regulatory Authority
• Conduct mock GMP audits as per specific requirements
• Prepares Drug Master Files to support API manufacturers

• We can design world class facilities such as GMP-regulated manufacturing sites and scientific laboratories.
• Our engineering staff are experts in facility and clean room design and classification. They will ensure that work done on clean rooms adheres to the correct standards, helping to avoid costly mistakes.
• Our facility design review services will ensure regulatory compliance and efficient workflows within a facility.

• Pharmaceutical process validation to PIC/S, EU EMA and TGA regulations.
• Pharmaceutical equipment validation to international regulatory standards and in accordance with current Good Manufacturing Practice.
• Cleaning validation for pharmaceutical manufacturing facilities.
• Temperature mapping of warehouses, cold rooms and other temperature controlled spaces.

If you are exporting product to multiple countries that use different regulatory frameworks, we can help you achieve compliance in a practical way, rather than drowning yourself in paperwork. A GMP Compliance Audit will allow you to avoid delays in bringing product to market due to not passing a GMP audit. The cost and time associated with regulatory re-audits if an audit outcome is not satisfactory can also be avoided or minimised.

If you:

• are soon to be audited by a GMP regulator,
• want to ensure you are still compliant after major change, or
• just had a tough regulatory audit and are facing a very difficult audit close out, we offer two audit services that may assist you with ensuring GMP compliance.

Site audits and qualification of API manufacturers in compliance to ICH Q7, excipient manufacturers, contract manufacturers and suppliers, packaging and labelling contractors, warehouse contractors and contract laboratories.