MarYop Pharmaceutical Consultants

Integral Quality Experience

Best GxP Pharmaceutical Consultant service provider for Pharmaceuticals, Life Sciences, Medical Devices, Biotech, Clinical, CROs , Food and Chemical industries across Globe

MarYop Pharmaceutical Consultants (MPC)

Established in 2021, today, MarYop Pharmaceutical Consultants (MPC) is one of the leading and well-established pharmaceutical consultancy specializing purely in GMP up-gradation, Quality Auditing, Quality Compliance, and Regulatory Services for clients across the globe.

We have registered offices in Ahmedabad, Gujarat (INDIA) from where the company operates. Our consultants/ auditors are also based in other countries to cover the world’s top parts.

All our consultants/auditors and subject matter experts are highly qualified professionals with expertise varying from 12 to 25 years of core experience in Specialization.

OVERVIEW: MarYop Pharmaceutical Consultants (MPC) offers support across a range of needs such as consulting, audits, remediation and training. We have extensive experience in supporting clients throughout India and abroad, satisfying the local and regulatory GMP requirements.

KEY PERSONNEL: Highly experienced Personnel in their respective field associated with MarYop Pharmaceutical Consultants (MPC).

Compliance MATTERS

OUR VISION

We believe in core values of superior quality, transparency, ethical approach, confidentiality, zero conflict of interest, accountability, honesty and constant improvement. .

OUR MISSION

We aim to be the most competitive and the most productive service organization in the world. Our core competencies in Pharma GMP consultancy and Auditing.

OUR VALUES

We seek to be characterized by our passion, integrity, entrepreneurialism and our innovative spirit, as we continually strive to fulfill our vision.

OUR EXPERTISE

As a consultancy services, MPC is dedicated to supporting the pharmaceutical industry by sharing our knowledge and expertise.

SERVICES WE PROVIDE

GMP CONSULTANT

Our experts are addressing professionally and efficiently your various and demanding GMP requirements. We are able to offer individual niche solutions for your challenges as well as comprehensive packages that cover all your GMP requirements.

For start-ups, we provide the implementation of a quality management system with all mandatory documents (GMP & GDP). Furthermore, our team support the GMP-compliant definition of process steps and implementation with regard to rooms and equipment (GxP QMS, GAP Analysis, Qualification & Validation). With us, you obtain your manufacturing authorization and the corresponding GMP certificate within the shortest possible time and move your business idea forward as quickly as possible.

PLANT UP-GRADATION

If you already have the API or Formulation Plant which is approved by the local regulatory authority and if you want to expand your reach to regulated territories like USFDA, EMEA, MHRA, PIC/S, WHO etc. then you may choose for Plant Up-gradation Service.

Plant Up-gradation Includes the following:

Establishment of Proper scope for which regulation is being targeted.
GAP Audit of Existing Plant (API/Formulation)
Preparation of GAP Audit Report,
Preparation of CAPA Plan,
Identification of GAPs and making time bound milestones for up-gradation
Validation
SOP and Procedures up-gradation,
Training
QMS system establishment/ restructuring as per requirement
Internal Audit System development.
Training: Our qualified & experienced Trainers provide training on all GXP topics like GMP, GDP, GLP, Data Integrity, QMS and many other critical topics which helps to enhance employees skill and operational performance.

AUDITS: Independent Supplier Audit (GMP System and Facility Audit)

To evaluate the system and manufacturing facility in compliance with the regulatory expectation and quality standards. To ensure the capability of the facility to manufacture quality medicine. To determine the effectiveness of the Quality system implemented and adherence to the specified quality objectives.

Vendor qualification/assessment Audit
Remote Audit / Virtual Audit
Pre-Inspection Audit
GAP Audit
QMS Audit

REGULATORY

We MarYop Pharmaceutical Consultants (MPC) provides Dossier preparation and submission service. We provide innovative, cost-effective, and creative graphic design & artwork services to support new product launches and brand re-designs. Our artwork management team deals with artwork management of any product including leaflet, carton, and label.

We also offer artwork services for content to carton, labeling and primary and secondary packaging, which include all printed materials associated with the products e.g., containers, cartons, foils and inserts etc. MPC has an unsurpassed reputation for excellence in technical, regulatory consulting, and guidance services for the Pharmaceutical Industry, including generic and new drug products, OTC, and monograph drugs, and many more.

MPC is proficient in the development, implementation, and management of diversified projects involving compliance, scientific principles, technical aspects, and regulatory requirements related to pharmaceutical products.

QUALIFIED PERSON (QP)

We MarYop Pharmaceutical Consultants (MPC) provides the highest standard of Qualified Person (QP) services in the pharmaceutical industry.

We provide experienced QP resource to conduct routine QP activities such as contract QP services for both Commercial and IMP products and batch certification etc. More importantly we can partner our QP expertise with you to make your firms business and quality management systems inspection ready, efficient and effective.

GMP Projects-Formulations/APIs

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Audits-Formulations/APIs

Product Filling- CTD/eCTD

Recruitment- Consultants & Pharma SMEs