“Strengthen Your Quality System. Be Audit-Ready. Stay GMP Compliant”
AASP Lifesciences Pvt. Ltd. offers professional part-time Quality Assurance and GMP regulatory support to pharmaceutical and healthcare manufacturing organizations seeking experienced QA assistance without the need for a full-time resource.
🔹 OUR QA & GMP SUPPORT SERVICES
✅ GMP Audit Preparation & Audit Readiness
Prepare your facility, documentation, systems, and teams for upcoming regulatory, customer, and GMP audits.
✅ GMP Gap Analysis
Systematic assessment of your existing quality systems against applicable GMP requirements, with identification of gaps and recommended corrective actions.
✅ Regulatory Inspection / RBI Readiness & Gap Analysis
Support for preparation and readiness assessment for applicable regulatory inspections, including identification of potential compliance gaps.
✅ QA Documentation & Compliance Support
Assistance with reviewing and strengthening SOPs, quality systems, records, documentation practices, CAPA, deviation, change control, self-inspection, and related GMP systems.
✅ GMP Training for Plant Teams
Practical training programs for QA, QC, Production, Engineering, Warehouse, and other relevant personnel based on applicable current GMP requirements.
✅ Drug License Support
Professional assistance with documentation and regulatory processes for applicable drug manufacturing and related licenses.
✅ GMP Certification Support
Assistance with preparation and regulatory documentation for applicable GMP certification requirements.
✅ WHO-GMP / PIC/S / EU-GMP Readiness Support
Gap assessment, documentation review, audit preparation, training, and implementation support for organizations preparing for applicable international GMP expectations.
✅ GLP Compliance Support
Assistance with GLP-related systems, documentation, training, and compliance-gap assessment where applicable.
🏗️ NEW GREENFIELD PROJECT SUPPORT
Planning a new pharmaceutical manufacturing facility?
Our team can provide QA and regulatory support from the planning stage, including:
• Quality system planning
• GMP-compliant documentation framework
• Facility and process compliance review
• SOP and quality-system development
• GMP training
• Audit-readiness planning
• Regulatory documentation support
• Pre-inspection readiness assessment
🔄 BROWNFIELD PROJECT SUPPORT
For existing pharmaceutical facilities undergoing expansion, modification, modernization, or regulatory improvement, we provide:
• GMP gap assessment
• Quality-system strengthening
• Documentation review
• Audit and inspection readiness
• CAPA implementation support
• GMP training
• Regulatory compliance support
• Quality-system improvement planning
💼 WHY CHOOSE AASP LIFESCIENCES?
✔ Experienced QA & Regulatory Support
Practical assistance focused on pharmaceutical quality systems and regulatory expectations.
✔ Flexible Part-Time Support
Get professional QA support according to your organization’s requirements without necessarily maintaining a full-time consulting resource.
✔ Audit-Focused Approach
Prepare your organization before the auditor or inspector arrives.
✔ Practical GMP Implementation
Our focus is not only on documentation but also on practical implementation and personnel awareness.
✔ Support from Gap Assessment to Readiness
Identify gaps, develop an action plan, strengthen systems, train personnel, and prepare your team for applicable audits and inspections.
🚀 IS YOUR FACILITY AUDIT-READY?
Don’t wait until an audit or regulatory inspection is announced.
Prepare today. Identify gaps. Strengthen your systems. Train your team. Improve your GMP readiness.
AASP LIFESCIENCES PVT. LTD.
Part-Time QA • GMP Consulting • Audit Readiness • Regulatory Support
📍 2nd Floor, 6 C, Rally, Sector 12-A,
Panchkula, Haryana – 134112, India
📞 +91 82647 25769
📧 info@aasplifesciences.com
📞 CONTACT US FOR A CONSULTATION
Discuss your QA, GMP, audit-readiness, regulatory licensing, Greenfield, or Brownfield project requirements with our team.
Services are provided based on the applicable regulatory requirements, project scope, documentation, and engagement terms. Regulatory approvals and certifications remain subject to assessment and approval by the respective competent authorities.
