Excellence Through Every Process
Quality Systems
Ensuring Global Trust
Uncompromised Standards. Transparent Processes. Trusted Outcomes.
From raw material procurement to batch release, every step is guided by a quality-first mindset aligned with:
- WHO-GMP (Good Manufacturing Practices)
- Global pharmacopoeias (IP, BP, USP)
- CDSCO & international MOH regulatory frameworks
- ISO quality management systems
- Ethical and scientific best practices
Our partners trust us because our quality systems are predictable, reliable, and fully verifiable.
Global Compliance Through Robust Quality
A Quality System Built for Global Compliance
Aidotick Pharmaceuticals operates a comprehensive, multi-layered quality governance system that integrates Quality Assurance, Quality Control, and Quality Management, ensuring every process, documentation, and batch meets global compliance and scientific rigor.
Quality Assurance (QA)
Comprehensive process design, meticulous documentation, GMP compliance, deviation control, validation, change control, and batch certification.
Quality Control (QC)
Scientific testing of raw materials, in-process samples, and finished products using validated analytical methods.
Quality Management System (QMS)
A holistic platform ensuring continuous monitoring, documentation integrity, audit readiness, and corrective action processes.
Commitment To Consistent Excellence
Quality Assurance
Our Core Philosophy
Quality Assurance at Aidotick Pharmaceuticals emphasizes robust systems, not just results. Every process is:
- Defined
- Documented
- Controlled
- Verified
- Audited
- Continuously improved
This proactive approach builds lasting trust with distributors, healthcare providers, and regulatory authorities worldwide.
Ensuring Excellence From Start
Raw Material Verification
Ensuring Consistent Quality
Every product’s quality starts with the ingredients used. Aidotick Pharmaceuticals enforces a strict Vendor Qualification Program, including:
- Supplier audits
- GMP compliance verification
- Material specification approval
- Consignment-by-consignment quality testing
- Approved vendor list (AVL) monitoring
Scientific testing includes:
- Identity confirmation
- Purity analysis
- Assay validation
- Microbiological examination
- Heavy metal checks
- Solvent residue tests
Only materials meeting predefined standards proceed to manufacturing, ensuring safe, reliable, and high-quality products.
Continuous Monitoring Ensures Reliable Production
In-Process Quality
Controls Ensuring Excellence
During every production stage — blending, granulation, compression, filling, sealing, and packing — our IPQC team conducts continuous monitoring.
Key parameters evaluated include:
- Weight variation
- Disintegration time
- Hardness
- Moisture content
- Viscosity (for liquids)
- pH levels
- Volume accuracy
- Sterility testing (where applicable)
This approach ensures real-time quality control, reduces deviations, and guarantees consistent batch uniformity across all products.
Ensuring Every Product Meets Standards
Finished Product Testing
for Assured Quality
Before any batch is released, it undergoes extensive laboratory testing in our QC analytical and microbiology labs.
Tests performed include:
- Assay (API content)
- Dissolution profile
- Related substances
- Friability
- Uniformity of content
- Microbial limit tests
- Sterility (for injectables)
- Stability testing
- Visual inspection for defects
Only after meeting all parameters is a Certificate of Analysis (COA) issued by our QA team, ensuring safe, reliable, and high-quality products.
Built to Meet Global Standards
WHO-GMP Aligned
Manufacturing Ecosystem
All Aidotick Pharmaceuticals products are manufactured within a licensed WHO-GMP–compliant environment, ensuring:
- Hygienic, well-controlled facility design
- Validated equipment and manufacturing processes
- Trained and qualified personnel
- Documentation-driven operations
- Monitored environmental conditions
- Strict cleaning and sanitation protocols
This manufacturing framework supports global regulatory approvals and ensures every product consistently meets international quality expectations.
Aligned With Global Pharmacopoeias
Pharmacopoeial Alignment
for Global Registrations
Aidotick formulations are developed and manufactured in strict alignment with international pharmacopoeial standards, including:
- IP – Indian Pharmacopoeia
- BP – British Pharmacopoeia
- USP– United States Pharmacopoeia
This alignment enables smooth product registrations across multiple regions and strengthens regulatory confidence in diverse global markets.
Engineered Quality Through Validation
Quality Validation
and Qualification Systems
Aidotick’s validation framework includes:
Process Validation:
Ensures every manufacturing step consistently produces batches meeting predefined quality specifications.
Equipment Qualification:
- IQ– Installation Qualification
- OQ– Operational Qualification
- PQ– Performance Qualification
Cleaning Validation:
Confirms effective cleaning procedures to prevent cross-contamination between batches.
Analytical Method Validation:
Verifies accuracy, precision, specificity, linearity, and reproducibility of all testing methods.
Computer System Validation:
Ensures digital platforms such as LIMS, ERP, and QMS operate with full data integrity and compliance.
Transparent Records. Complete Traceability.
Controlled Documentation
for Regulatory Confidence
Regulatory authorities evaluate organizations by the accuracy, consistency, and reliability of their documentation. Aidotick Pharmaceuticals maintains strict documentation controls, including:
- Batch Manufacturing Records (BMR)
- Batch Packaging Records (BPR)
- SOP-driven operational processes
- Equipment and utility logbooks
- Controlled change management systems
- Transparent documentation of deviations, CAPA, and investigations
Every activity remains fully traceable, audit-ready, and aligned with international regulatory expectations.
Proven Stability for Market Confidence
Stability Studies and
Shelf-Life Determination
Aidotick conducts ICH-guided stability studies to establish accurate product shelf-life under:
- Accelerated storage conditions
- Long-term storage conditions
- Zone IV climatic conditions, common across Africa and Asia
These studies are essential for:
- Regulatory registration dossiers
- Ministry of Health submissions
- Strategic market expansion
- Partner confidence in long-term product durability
Precision Testing Backed by Science
Microbiological & Analytical
Laboratory Excellence
Our QC laboratories are equipped with advanced analytical and microbiological instruments, including:
- HPLC (High Performance Liquid Chromatography)
- UV-Visible Spectrophotometer
- Dissolution Testers
- Disintegration Testers
- Friability Testers
- pH Meters
- Stability Chambers
- Microbiology LAF (Laminar Airflow) Systems
These facilities ensure accurate, repeatable, and globally acceptable testing results that meet international quality and regulatory standards.
Always Prepared. Always Transparent.
Audit Readiness &
Regulatory Transparency
Aidotick maintains continuous audit readiness for:
- Internal quality audits
- External partner audits
- Regulatory inspections
- Third-party GMP assessments
- Comprehensive documentation verification
This level of transparency strengthens our credibility with Ministries of Health, importers, and institutional buyers across global markets.
Quality Embedded in Every Action
A Culture of Quality
Across Organization
Quality is deeply embedded across the Aidotick organization through:
- Ongoing training programs
- Regular GMP workshops
- SOP review and refresh cycles
- Skill development initiatives
- Continuous improvement programs
Our teams don’t work toward quality — they operate from quality, every day, at every level.
Built on Trust and Transparency
Reliable Quality
Systems for Partners
or every partner working with Aidotick Pharmaceuticals, we deliver:
Quality You Can Trust
Scientifically validated, compliant, and consistent products meeting global standards.
Documentation You Can Rely On
Complete and accurate COA, COPP, stability reports, GMP certificates, product dossiers, and validation reports.
Processes You Can Verify
Transparent operations aligned with international audit and regulatory requirements.
Support You Can Build On
Ongoing regulatory, technical, and scientific support throughout product registration and market expansion.
Quality is not just what we promise it is how we work every day
At Aidotick Pharmaceuticals, we are committed to delivering medicines that meet the highest global standards of safety, reliability, and scientific integrity.
Through disciplined quality systems and an unwavering focus on excellence, we continue to build lasting trust with partners and healthcare systems worldwide.