GMPPro comes with many features which are strongly recommended to Drug / Food manufacturing companies.

Business Benefits

Industry Best Practices

MottoSystems’ prides on a perceptive approach to its work that realizes error free, stringent and easy to implement Quality Management Systems every time. The team of qualified subject matter experts at MottoSystems’ interacts with personnel of relevant departments before setting out to design systems that augment best practices at all levels.

Controlled Environment

GMPPro ushers stringent compliance regimes where deviations from Standard Operating Procedures become almost extinct. It lends control over document distribution and access, enables supplier control through effective evaluation and effectively reigns in rejections and non-conformities to catalyze overall profitability of the organization.

Connected Processes

MottoSystems’ appreciates the need for effective coordination and communication at inter and intra department levels for realizing overall efficiency, and GMPPro achieves this by bringing various functions on to one integrated platform while eliminating silos between departments and the ensuing data duplication for improved data integrity

Improved Compliance

GMPPro works intelligently for data delegations and validations. By reducing manual dependencies it improves ease of data administration during investigations, review, analysis & trending of data.

Cost Reduction

GMPPro saves great in terms of both money and time. Not only it disposes off with the onerous manual entries but also acts as your ready reckoner during data vertification & reporting in addition to facilitating timely delivery to customers. Not to mention the cost of production reruns in case of non-compliance to procedures.

Key Features

  • 21 CFR Part 11 compliance for Electronic Records & Signatures.
  • 21 CFR Part 210 & 211 compliance for cGMP Practices.
  • Customizable workflows as per company SOPs.
  • Built-in cGMPs to achieve compliance at every level.
  • Automated Notifications via dashboard widgets and emails.
  • Auto escalation of tasks, reports and complaints.
  • Integrated change management throughout process cycle.
  • Self-driven navigation and user friendly screens.
  • Drill-down data architecture for effective investigations.
  • Harmonized best practices and guides users to follow as per SOPs.
  • Advanced search options and retrieval of intended data.
  • Complete control on rejected & expired materials for usage.
  • Version controls and access controls over obsolete documents.
  • Secure and role based access to each module.
  • Complete data security & automated data backup.
  • Complete Audit Trail.

Advantages at all levels in the organization

  • Automated communication between departments for immediate, effective & responsive tasks.
  • Secure & reliable data reports for error free audits.
  • Harmonized procedures for better performance.
  • Easy and Control access on documents
  • Complete control over the Company’s quality practices.
  • Clearly defined and controlled procedures for consistent performance.
  • Unique repository for all quality management system documents.
  • Saves time for employees during document preparation, handling, archiving & retrieving.
  • Dynamic data reporting to generate Annual Product Reports (APR).
  • Data backup system which can be retrieved and saved.
  • Powerful User Management System.

GMP Compliance for Life Science Industries

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