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PLAY VIDEO SOFTWARE FOR COSMETICS BUSINESSES Internal Audits| GMP ISO:22716

Complete solution for ISO 22716 compliance

The ISO 22716 standard requires a comprehensive approach and quality management system for those engaged in the manufacturing, packaging, testing, storage, and transportation of cosmetic products.

Kosmetikk Laboratoriet

Having Cosmetri GMP makes the whole process of complying to ISO:22716 as a business look like a walk in the park. Extremely helpful and committed people working at Cosmetri!

Stephan Ulvund Øien

Product Developer & Colorist - Kosmetikk Laboratoriet

CR Formulations

Cosmetri is without doubt the most comprehensive and user-friendly compliance software for our industry. We used it to obtain and maintain our GMP ISO 22716. From the management of raw materials to final batch protocols the system just delivers.

Tim Burt

Operations Manager - CR Formulations

GE Organics Ltd

We are really happy with the software, its well constructed, has a great user interface, and was developed with a clear understanding of the requirements of ISO 22716 GMP. Georganics would highly recommend it for any cosmetics company that is looking for a high quality, comprehensive GMP software.

Ryan Garratt

Quality Administrator - GE Organics Ltd

Green Angel Skin Care

We are a skin care manufacturer and cosmetri is an invaluable piece of software that is central to our manufacturing processes. The service is fantastic, and queries are dealt with in a timely and helpful manner.

Philip Devery

Compliance & Development - Green Angel Skin Care

Ginkel's Cosmetica

Today we had an annual audit from the Dutch health inspection team. They were very enthusiastic about our implementation of cosmetri for achieving compliance with cosmetic Cosmetics Good Manufacturing Practices (GMP) ISO:22716.

Christian Nauta

CEO - Ginkel's Cosmetica

cosmetri GMP is an affordable turnkey solution enabling rapid deployment and minimal disruption to your business. Features of the software include:

  • Rapid deployment - be operational within 2-3 days
  • Comprehensive coverage of ISO:22716
  • Fully configurable
  • Optimized for tablet and PC devices
  • Integrated electronic document management
  • Email notifications
  • Department and role-based user management
  • Integrates with cosmetri Product Manager, or standalone
  • Change logs
  • Scalable for any company size, from 5 to 5,000+ users
  • Dedicated database and FTP
  • Export full document archive
  • Data backup (cloud-hosted version)
  • 2 x 1-hour online-training sessions included in plan

ISO 22716 GMP compliance software features


cosmetri GMP includes the following:

ISO 22716 GMP internal audit

Internal Audits

Form-based audit questionnaires cover every section of ISO 22716. Tablet-optimized for easy on-premise inspections and upload of photographic evidence. Review associated GMP documents and report issues requiring a CAPA response.

ISO 22716 GMP CAPA

CAPA

Report and track risk-assessed deviations throughout every aspect of the business workflow. Issues can be escalated to require a CAPA or SCAR corrective action. Authorized users can participate in a discussion to resolve each issue.


Document Management

Full electronic document management for ISO 22716, including SOP and WI management. 30 included SOP templates. Associate a GMP document with any item. Supports e-signed PDF documents. Export complete document archive.

Product Recalls

Template-based recall management with mail-merge features for efficient generation of recall documents. Track send/receive history, import customer/distributor sales data and manage communication with recall authorities.


ISO 22716 GMP user management

Staff Management

Efficient administration of staff and permissions using department/role-based logic. View user activity logs and set chains of command. Out-of-the-box configuration for ISO 22716 with the option to add custom departments and roles.

ISO 22716 Out of Specification OOS

OOS Investigations

Report an out-of-specification for any product/formula/batch. Complete Stage 1 to identify associated tests. Escalation to Stage 2 requires re-testing with resultant CAPA and conclusions.


ISO 22716 Customer Complaints

Customer Complaints

Enter and manage the complaint process through to resolution. View complaints by customer, product, batch, status and assessed risk. Associate a complaint with a SUE or OOS.

ISO 22716 GMP supplier reviews

Supplier Reviews

Automate the GMP review process for suppliers and sub-contractors, including supplier document management. Supports supplier-type Issues with required SCAR resolution.


ISO 22716 GMP Sue management

SUE Management

Extend GMP ISO 22716 to manage and report SUEs that can be triggered from an OOS, Product Recall or Customer Complaint. Generate an SUE notification report, including EU-compliant format.

ISO 22716 GMP KPIs continual improvement

Reporting & KPIs

View key statistics and reports and assess current risk level of open items. Gain insights into your company's performance, facilitating continual improvement.





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