Addsum Lifesciences – One Step Towards Life

Pharma

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Healthcare solutions across multiple segments

Welcome to Addsum Lifesciences

Advancing Healthcare, Enhancing Lives

At Addsum Lifesciences, we are committed to delivering high-quality pharmaceutical, nutraceutical, and healthcare solutions that improve patient outcomes and support healthier communities. Guided by innovation, integrity, and excellence, we strive to provide safe, effective, and affordable products that meet the evolving healthcare needs of India.

Our Core Strengths

Trusted Quality, Growing Nationwide

Quality-Driven Manufacturing

We work with WHO-GMP certified manufacturing facilities through a reliable third-party manufacturing model to ensure the production of high-quality pharmaceutical products. Every product undergoes stringent quality assurance and regulatory compliance processes to meet established standards of safety, efficacy, and consistency. Our commitment to quality enables us to deliver dependable healthcare solutions while building long-term trust among healthcare professionals and patients across India.

Our Process

At Addsum Lifesciences, quality is integrated into every step of our manufacturing process. From raw material inspection and laboratory testing to production, packaging, and final product release, each stage follows stringent quality control procedures and GMP standards to ensure safe, effective, and reliable pharmaceutical products. Explore the process flow charts below to understand our commitment to quality and compliance.

Raw Material Inspection Flow Chart

Raw Material Receipt

All incoming raw materials are received from approved vendors and verified with purchase documents. Each batch is assigned a unique identification for complete traceability before quality inspection begins.

Verification & Sampling

Our Quality Control team verifies the material identity, packaging, labeling, and quantity. Representative samples are collected using standard sampling procedures to ensure accurate laboratory analysis.

Laboratory Testing

Collected samples undergo comprehensive quality evaluation according to approved specifications.

Testing includes:

In-house Testing: Physical, chemical, and microbiological analysis in our QC laboratory.
External Testing: Specialized or regulatory tests are performed by NABL/approved external laboratories whenever required.

Quality Review & Decision

All laboratory reports are reviewed by the Quality Assurance team before making the final release decision.

Final Outcome:

Approved: Materials meeting all specifications are released for manufacturing.
Rejected: Non-conforming materials are rejected, documented, and returned to the supplier as per quality procedures.

Packaging Material Inspection Flow Chart

Packaging Material Receipt

All packaging materials are received from approved suppliers and checked against purchase documents. Each batch is identified, recorded, and prepared for quality inspection to ensure complete traceability.

Verification & Sampling

QC Verification & Sampling

The Quality Control team verifies the packaging material for quantity, labeling, dimensions, and physical condition. Representative samples are collected according to approved sampling procedures for quality evaluation.

Laboratory Testing

Testing as per Specifications

The collected samples are tested according to approved quality specifications to verify their compliance with pharmaceutical packaging standards and regulatory requirements.

In-House Testing

In-House Quality Testing

Our Quality Control laboratory performs detailed inspections of the packaging material, including appearance, dimensions, print quality, strength, and other critical quality parameters.

Quality Review

Results Review & Final Decision

The Quality Assurance team reviews all testing results before making the final decision. Packaging materials that meet all specifications are approved for manufacturing, while non-conforming materials are rejected and returned to the supplier following standard quality procedures.

In-Process Inspection Flow Chart

Inspection Request

In-Process Inspection Request

The Production department submits an inspection request to the Quality Assurance team at predefined stages of the manufacturing process to ensure compliance with approved procedures.

QA Inspection

Quality Assurance Inspection

The Quality Assurance team performs in-process inspections to verify that manufacturing activities are carried out according to approved SOPs, batch records, and quality standards.

Process Testing

Testing as per Specifications

Samples collected during production are tested according to approved specifications to evaluate critical quality parameters and ensure the process remains within established limits.

Results Review

Quality Results Review

All inspection observations and test results are carefully reviewed by the Quality Assurance team to confirm compliance with quality requirements before proceeding further.

Production Approval

Communication to Production

The reviewed inspection results are communicated to the Production department. If all quality requirements are met, production continues. Any deviations are reported immediately, and corrective actions are initiated before the manufacturing process proceeds.

Completion of Batch of Finished Products at Manufacturing Site

Batch Completion

Finished Product Batch Completion

Once the manufacturing process is completed, the finished product batch is transferred for final quality inspection. Each batch is identified, documented, and prepared for sampling according to approved quality procedures.

Verification & Sampling

QC Verification & Sampling

The Quality Control team verifies the finished product batch, checks packaging details, labeling, and documentation, and collects representative samples following approved sampling procedures for quality evaluation.

Laboratory Testing

Testing as per Specifications

Collected samples undergo comprehensive quality testing in accordance with approved specifications to ensure the finished product meets all safety, quality, and regulatory requirements.

Testing includes:

In-House Testing: Physical, chemical, microbiological, and other routine quality tests are performed in our Quality Control laboratory.

External Testing: Specialized or regulatory tests are conducted through approved external laboratories whenever required.

Quality Review

Results Review & Final Decision

The Quality Assurance team reviews all laboratory reports before releasing the final batch.

Final Outcome:

Approved: Finished products that comply with all specifications are approved for dispatch.

Rejected: Products failing to meet quality standards are rejected and processed for safe destruction in accordance with approved quality and regulatory procedures.