GMPPro logo

GMPPro

by Motto Systems · Since 2013
No reviews yet
ActiveAvailable globallyCloud
Quick facts
VendorMotto Systems
Year launched2013
StatusActive
Location1st Floor, Samridhi Vasyam, Jaihind Colony, Madhapur, Hyderabad - 500 081. Telangana. India.
Countries servedGlobal
Languages5
IntegrationsN/A
Free tierN/A
Free trialN/A
Contact salesYES

About GMPPro

GMPPro is a pharma QMS software from Motto Systems that manages quality policies for pharmaceutical manufacturers. It includes features such as Company Profile, Vision/Mission/Work Culture, and Our Offerings so users can effectively oversee compliance and maintain quality standards. This software suite is designed to support the unique needs of the pharmaceutical industry, ensuring that all quality management processes are well-documented and accessible. GMPPro integrates various functionalities to assist organizations in adhering to regulatory requirements and improving operational efficiency. Key capabilities: Quality Management Compliance Tracking Document Control Training Management Audit Management Best for: pharmaceutical manufacturers that need reliable quality management solutions.

GMPPro by Motto Systems is a robust Quality Management Software (QMS) designed to help organizations in highly regulated industries streamline their quality and compliance processes. The software is particularly well-suited for pharmaceutical, biotech, food and beverage, and medical device companies, ensuring that they meet Good Manufacturing Practices (GMP) and other regulatory standards. By offering a comprehensive suite of tools, GMPPro enables businesses to maintain compliance, improve product quality, and enhance operational efficiency. Some of its core functionalities include document control, audit management, corrective and preventive actions (CAPA), training management, supplier quality management, and risk assessment. Its cloud-based deployment model ensures accessibility and scalability, making it an ideal solution for companies of various sizes. The user interface of GMPPro is designed with usability in mind, offering an intuitive and structured layout that allows users to navigate through different modules with ease. The dashboard provides a centralized view of key metrics, ongoing quality processes, and compliance status, ensuring that users can quickly access critical information.

Pros & Cons

Pros
  • Web-based and easy to use.
  • Good for documenting and improving processes.
  • Customizable to SOP requirements.
  • Excellent customer support and helpful team.
  • Comprehensive for managing quality in the pharma industry.
Cons
  • Features rating is listed as 0.0 on the main page, which is unusual and might indicate missing data or a platform issue. (This is an observation from the Capterra listing, not directly from the user reviews).
  • One review mentioned it's excellent for managing inventory (though this might not be its primary focus).

Features

Key features

Comprehensive Pharmaceutical PLM Software

Encompasses production, quality control, quality assurance, and engineering.

Systemic Integration

Integrates various aspects of pharmaceutical operations.

Independent Solution Modules

Offers modules that can be used individually.

Regulation Abiding Solution

Complies with pharmaceutical regulations.

Easy to Use and Adaptable

User-friendly and can be tailored to specific needs.

Balanced Metrics and Dependable cGMP Controls

Provides relevant metrics and built-in controls for current Good Manufacturing Practices.

Applicable to All Pharmaceutical Companies (Small to Large)

Suitable for businesses of varying sizes.

Responsive to Company SOPs

Adapts to the Standard Operating Procedures of individual companies.

Integrates Departments

Connects different departments within a defined closed-loop Product Lifecycle Management (PLM) system.

Combines Internal and External Regulations

Integrates both internal company policies and external regulatory requirements.

Conforms to 21CFR Part 210 & 211 and 21 CFR Part II Certifications and Norms

Meets specific FDA regulations.

Designed for Total Control of Processes

Provides tools for managing and overseeing pharmaceutical processes.

Backed by Industry-Focused Professional Team

Supported by experts with experience in the pharmaceutical sector.

Abreast with Regulatory Compliance's, Trends, and Challenges

Keeps up-to-date with the latest regulatory landscape.

Advanced PLM Suite Dealing with Complex Instructions Easily

Simplifies the management of complex pharmaceutical quality instructions.

Order of Specific Need-Driven Solutions

Offers solutions tailored to specific requirements.

Quality Management System (Integrated Solution)

Manages quality processes.

Laboratory Information Management System (Integrated Solution)

Manages laboratory data and workflows.

Document Management System (Integrated Solution)

Controls and organizes documents.

Training Management System (Integrated Solution)

Manages employee training records and processes.

Audit Management System (Integrated Solution)

Facilitates the planning, execution, and tracking of audits.

Additional features

Specifically designed and developed for the life science and pharmaceutical industries

Tailored to the unique needs of this sector.

Integrative quality management system

Provides a unified approach to quality management.

Resolves quality issues at any stage of drug development

Addresses quality concerns throughout the product lifecycle.

Capable of encompassing the whole spectrum of production, quality control, quality assurance, and engineering

Covers all critical functional areas.

Systemic integration

Connects different processes and data points within the system.

As independent solution modules as well

Offers flexibility to use modules separately if needed.

Regulation abiding solution

Ensures compliance with relevant pharmaceutical regulations.

Ideal in features

Offers a comprehensive set of functionalities.

Easy to use

User-friendly interface for efficient operation.

Adaptable

Can be customized to meet the specific requirements of different organizations.

Balanced metrics

Provides relevant and meaningful performance indicators.

Dependable built-in cGMP controls

Includes controls to ensure adherence to current Good Manufacturing Practices.

Complete solution applicable to all pharmaceutical companies small to large

Scalable for businesses of any size.

Responsive in respect to SOPs of the companies

Can be configured to align with company-specific Standard Operating Procedures.

Integrating departments to clearly defined closed-loop PLM

Facilitates collaboration and information flow between departments within a structured PLM framework.

Combining seamlessly all internal and external regulations

Integrates both company policies and external regulatory requirements.

Conforms to 21CFR Part 210 & 211 and 21 CFR Part II certifications and norms

Meets specific FDA regulations related to drug manufacturing and electronic records.

Designed for total control of processes

Provides tools and visibility to manage and monitor all relevant processes.

Backed by our industry-focused professional team extensively experienced across the pharmaceutical sector

Supported by knowledgeable experts.

Abreast with regulatory compliance's, trends and challenges

Stays updated with the latest regulatory changes and industry trends.

The team guides direction towards fulfilling the set quality specifications

Provides expertise to help achieve quality goals.

Advanced PLM suite dealing complex pharmaceutical quality instructions easily

Simplifies the management of intricate quality requirements.

With an order of specific need-driven solutions

Offers tailored solutions to address specific challenges.

Quality Management System

A module for managing overall quality processes and standards.

Laboratory Information Management System

A module for managing laboratory samples, tests, and results.

Document Management System

A module for controlling, organizing, and tracking documents.

Training Management System

A module for managing employee training records, schedules, and compliance.

Audit Management System

A module for planning, conducting, and tracking audits.

Pricing

Free trial
Free version
Request a quote
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Countries & Languages

Global
Countries served
5
Interface languages
7
Billing currencies

Interface languages

EnglishSpanishFrenchGermanItalian

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇦🇺AUD🇨🇦CAD🇯🇵JPY🇨🇳CNY

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