Pharma & Bio-Pharma Quality Systems and Compliance

Compliance is a journey, it starts today and will evolve in future. In today’s world the challenge comes from being compliant to US FDA and other regulators. Not addressing some of the underlying concerns of Quality Systems and Compliance will create a hurdle in your journey, sooner or later it may come up as FDA 483s or FDA warning letters. The outcome of such hurdles are often devastating such as halt in production, product recall, certain import bans, document detention or product seizure, which may have negative impact on your organization and may damage your organization’s reputation, pipeline products. This will also affect financial well-being and market reputation.

Keeping up your company on quality systems and compliance to match with the constantly changing regulatory guidelines released by regulatory authorities around the world, is a challenge. At MS Remedies Inc. we understand this challenge and provide you service to keep up to date with your compliance status. We have experience in creating, modifying, reviewing, implementing and remediating quality systems for Pharma and Bio-Pharma organizations. MS Remedies wants to serve your organization to answer any question or issues related to quality systems.

Contact MS Remedies Inc. at +1-647-229-7236 or

At MS Remedies, we utilize a systems-based approach to compliance:

  • Quality system
  • Laboratory controls
  • Material controls
  • Facilities and equipment
  • Production system
  • Packaging and labeling

We will serve your organization to provide you following services:

  • Gap Assessments – Details to be added later
  • Risk Assessments – Details to be added later
  • Corrective Action Plans – Details to be added later
  • Remediation – Details to be added later