Product Safety & Quality Compliance Statement
1. Overview
Ballia Corpus is committed to delivering products that meet rigorous safety and quality standards. Although the Lyonsbarry.com Portal itself does not involve product sales, clients use it to request manufacturing services for goods destined for consumer markets. The following practices illustrate our dedication to product safety, regulatory compliance and continuous improvement.
2. Compliance with Good Manufacturing Practices (GMP)
Our manufacturing facilities operate in accordance with applicable Good Manufacturing Practice (GMP) regulations, such as those established for dietary supplements and cosmetics. We maintain master manufacturing and batch production records, verify the identity, purity, strength and composition of each ingredient and follow proper packaging and labelling protocols. Records are retained for periods required by law to demonstrate compliance and facilitate traceability.
We operate under a documented Quality Management System covering:
Good Manufacturing Practice (GMP): Compliance with national and international GMP standards (FSSAI Schedule IV for India, US FDA 21 CFR 111/210, EU GMP, etc.).
ISO Standards: Implementation of ISO 22000 (Food Safety), ISO 22716 (Cosmetic GMP) and ISO 9001 (Quality Management).
Hazard Analysis & Critical Control Points (HACCP): Identification and control of hazards throughout production.
Regular Audits: Internal and external audits to verify compliance with regulatory and client requirements.
Quality Control Stages
Raw Material Authentication: All ingredients are tested using validated analytical methods (HPLC, GC‑MS, FTIR) to ensure identity and purity.
In‑Process Quality Checks: Continuous monitoring at critical control points during blending, filling and packaging.
Finished Product Verification: Potency, stability and packaging integrity tests to confirm compliance with label claims and shelf‑life requirements
Documentation & Traceability
We maintain batch production records, Certificates of Analysis (COAs), stability reports and technical dossiers for every lot. Digital systems (ERP and eQMS) ensure real‑time batch tracking and regulatory‑ready documentation
3. Ingredient and Finished Product Testing
We source raw materials from vetted suppliers and require certificates of analysis to confirm identity and purity. Finished products undergo quality control tests for potency, microbiological contamination, heavy metals and other relevant parameters. Tests are performed in accredited laboratories, and results are reviewed by quality assurance personnel before release.
4. Label Accuracy and Regulatory Compliance
We ensure that product labelling for bioactive naturals, plant based and skin care products meets applicable regulations, including accurate ingredient lists, net quantity, directions for use and appropriate cautionary statements. Health‑related claims are supported by scientific evidence and do not mislead consumers. Clients are responsible for adapting labels to meet the regulatory requirements of their target markets.
5. Post‑Market Monitoring and Adverse Event Reporting
We maintain systems to track customer feedback and report serious adverse events to relevant authorities where required. We cooperate with clients in the event of recalls, market withdrawals or safety notices, working to mitigate risks and protect public health.
6. Continuous Improvement
Quality management is a continuous process. We conduct internal audits, review manufacturing processes, train personnel and invest in technologies that enhance product safety and quality. Clients are welcome to audit our facilities by prior arrangement and subject to confidentiality agreements.
7. Contact for Product Safety and Quality
Ballia Corpus
SCO‑262, Business HUB, New Briz ‑ 2
Taraori, District Karnal, State Haryana – 132116, India
Email: care@Lyonsbarry.com
