Modular Pharma

Modular Pharma Co. is LLC Firm that has been operating within MENA region as a pharma industry project provider, consultant and partner for supplying of innovative equipment & quality materials.
We ensure pharma manufacturing partners to get the required support for technical projects, GMP consultation, pre inspection audits & training programs. In addition, Modular presents multinational vendors for active & inactive pharmaceutical ingredients, primary packaging materials, manufacturing equipment, production lines and manufacturing tools & accessories. Modular is a professional & technical expert in pharma industry sector & performs pharma-based business toward its client within regulated markets in MENA region.
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Why Modular

Modular Scopes

2 home scope material

Materials

Modular establishes a partnership business with primary packaging & raw materials vendors who already exist in US, Europe & regulated markets.
We present wide range of primary packaging PP solutions from global vendors who maintain GMP & ISO Quality standards to cover scopes of blister, tubes, jars, bottles & injectables,

Our range of raw includes providing support of offering new APIs & formulation dossiers as well against scopes of generics, new potent & near patency for human medicine, cosmetics & healthcare scope.

 

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Machinery

Modular works along with global partners who provide manufacturing and packaging lines, equipment & pharma tools as cGMP Complaint for the range of lab scale up to large volume production scales.

– Solid Dosage form (Tablet, Capsules & Powder).
– Liquid Manufacturing & Packing line.
– Cream Manufacturing & Packing line.
– Suppository Manufacturing & Packing line.
– Injectable line.

4 home scope project

Projects

Modular offers a broad technical portfolio for new pharma projects, new expansions & existing manufacturing firms as well.

Modular practices cGMP compliance evaluation toward manufacturing sites for proper design, monitoring & control of manufacturing processes in order to fulfil requirements based on USFDA, EU & WHO guidelines.

Modular provides training options for GMP regulated organizations. It includes manufacturers & related industries. An advantage of our in-house training courses is that the program, training content and methodology can be adapted to suit the specific needs that are of shopfloor driven base.

  • cGMP Current Good Manufacturing Practices.
  • Auditing & Self Inspections.
  • Audit Systems.
  • QMS Quality Management Systems.
  • Production & Engineering systems.

Materials

Modular establishes a partnership business with primary packaging & raw materials vendors who already exist in US, Europe & regulated markets.

We present wide range of primary packaging PP solutions from global vendors who maintain GMP & ISO Quality standards.

Some of PP solutions include:

1 – Alu – PVC/PVDC Blister packing solutions for tablet, Capsules, powder & Suppository.

2 – Tubes of Alu, Laminated & PE.

3 – Container & closures for solid & liquid dosage forms.

4 – Vials, ampules, rubber stoppers and aluminum seals.

We share ideas with our manufacturing clients & offer them new APIs & formulation dossiers sourcing solutions of US & Europe pharma standards that include USFDA, BP, EP along with CEP grade & DMF, we provide the required support for establishing new vendor approval as part of risk management policy & we ensure the best pricing & optimum delivery as well.

Our range of APIs includes commercial generics, new potent & near patency for human medicine, cosmetics & healthcare and for veterinary scope.

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MACHINERY

Modular works along with global partners who provide manufacturing & packaging lines, equipment & pharma tools of GMP Complaint for the range of lab scale up to large volume medicine production.

We ensure clients to have state of art innovative technology with best quality, best price & optimum capacity as well that suit for lines of:

• Granulation & blending.
• Tableting.
• Encapsulation.
• Coating.
• Blister packing.
• Counting.

• Metal Detector systems (For Powder, Tablet, Capsules & Jars).
• Check weighers (For Jars & Packs).
• Cameras & Pin Hole Detectors (For Tablet & Capsule in Blister).

• FBD Bag Filters.
• Powder Processing.
• Press Tooling of Premium steel with HCP & CrN Coating tips.
• Powder processing sieves.
• Liquid processing sieves.

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Projects

Modular offers a broad technical portfolio for new pharma projects, new expansions & existing manufacturing firms as well.

We understand partner needs & do customized analysis so can help firm owners to build up best user requirement specification URS for the working place, product, equipment & process.
This is in addition to build up an efficient operation system, quality practice and highly skilled manpower.

Modular offers a broad technical portfolio for new pharma projects, new expansions & existing manufacturing firms as well.

  • Establish Conceptual design as per cGMP.
  • Analyze & recommend new expansion Projects.
  • Plan, arranging & control of Turnkey Projects.
  • Measure & control shop floor management.
  • Determine required Process KPIs.
  • Execute continuous Training Programs.

Modular practices cGMP compliance evaluation toward manufacturing sites for proper design, monitoring & control of manufacturing processes in order to fulfil the requirements based on USFDA, EU & WHO guidelines.
We do pre inspection audits to assure the identity, strength, quality, and purity of drug products through establishing an adequately control manufacturing operations that prevent contamination, mix-ups, deviations, failures, and errors.

– Excellence of operations (Quality along with productivity).

– Establishing strong quality management systems.

– Obtaining appropriate quality raw materials.

–  Establishing robust operating procedures.

–  Detecting and investigating product quality deviations.

–  Continuous training programs.

Modular provides training options for GMP regulated organizations. This includes manufacturers, distributors, laboratories and related industries. An advantage of our in-house training courses is that the program.

  • Good Manufacturing Practices.
  • Auditing & Self Inspections.
  • Internal & External Auditing.
  • Auditing API / Excipient Suppliers.
  • Documentation / System Management.
  • Setting up a CAPA System.
  • Processing control: Production & Engineering
  • 3 Levels GMP schedules: Operators, Heads & Managements.
  • Quality Culture & Awareness
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