Validation

Validation Services by PROVAL

Your Partner in Compliance and Quality

At PROVAL, we are a full-service validation support firm with a team of highly skilled experts specializing in every aspect of pharmaceutical validation. Our services cover a range of compliance areas, from commissioning process and cleaning validation. As a local company, we offer quick response times, a deep commitment to quality, and budget-friendly pricing.

CALL US NOW : (877) 393-2437

Why Choose PROVAL?

Experienced Validation Experts

Our consultants bring years of experience in all areas of validation compliance, ensuring you have access to industry best practices and insights.

Quick, Local Support

We can be there when you need us most, minimizing delays and reducing travel costs for unbeatable value.

Quality Metrics

PROVAL takes pride in a history of high-quality service, meeting the complex demands of the pharmaceutical industry with precision and dedication.

Validation Services Support

We support the entire lifecycle of equipment qualification, from installation and commissioning to operational and performance qualification. Our experts ensure each piece of equipment meets regulatory requirements and functions as intended.

  • Installation Qualification (IQ): Verification that equipment is correctly installed per design specifications
  • Operational Qualification (OQ): Testing that confirms equipment operates within intended parameters.
  • Performance Qualification (PQ): Ensures that equipment performs consistently under actual production conditions.



Facility Qualification


Whether you are building a new facility or modifying an existing one, PROVAL provides end-to-end qualification services to validate that your facility meets regulatory standards and is capable of supporting pharmaceutical production processes.

  • HVAC Systems Ensuring air handling systems function effectively to control contamination and maintain appropriate environmental conditions.
  • Controlled Temperature and Humidity Testing that confirms equipment operates within intended parameters.

Utility Qualification


Our utility qualification services cover essential systems that support manufacturing, including HVAC, purified water systems, and process gases. We perform rigorous testing and qualification processes to ensure these utilities meet industry standards and function as intended

  • Purified Water Systems Verification of water quality to ensure it meets stringent purity requirements.
  • Process Gases Testing and validation to ensure gases are safe and effective for their intended use.

Process Validation


PROVAL follows a robust, three-stage process validation life cycle as per FDA guidelines. Our process validation services establish documented evidence that your manufacturing processes consistently produce products that meet quality standards.

  • Stage 1: Process Design Define the process and establish its robustness based on product requirements
  • Stage 2: Process Qualification Verify that the process performs as expected during production.
  • Stage 3: Continued Process Verification Implement ongoing monitoring to ensure the process remains in                control

Cleaning Validation


Cleaning validation is critical for preventing cross-contamination and ensuring product safety. PROVAL develops and verifies cleaning procedures, ensuring they effectively remove residues and meet pre-established acceptance criteria

  • Residue Limits and Acceptability Verification that detergent, excipients, and active ingredients are removed to safe levels.
  • Program Design Establish a customized cleaning validation program that meets industry standards and regulatory expectations.

Computerized System Validation (CSV)


In today’s digital age, computerized systems play a central role in manufacturing and quality control. Our CSV services ensure that all computerized systems are qualified according to the Good Automated Manufacturing Practice (GAMP5) guidelines, meeting cGMP, GLP, GCP, and 21 CFR Part 11 requirements.

  • Life Cycle Approach We follow a structured, life cycle-based validation approach that includes requirements, risk assessment, and validation.
  • Data Integrity Assurance Verification that systems maintain data integrity, security, and traceability throughout their use.

PROVAL

Flexible and Scalable Validation Support for Your Needs

Whether you are a small firm with limited validation resources, undergoing expansion, or responding to FDA audits, PROVAL is here to support you. With over a century of combined industry experience, our team offers validation expertise across all facets, from process and cleaning to equipment and facility qualification. Our personnel bring backgrounds from top pharmaceutical companies, making PROVAL the trusted partner to help you produce safe, effective, and compliant products every time.

Contact PROVAL for ReliableValidation Suppor

Ready to meet your validation needs? Partner with PROVAL for expert guidance, reliable support, and the highest standards of quality. Contact us today to discuss how we can support your validation compliance efforts Mapping