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Accueil Corporate Gouvernance

Structure et gouvernance d'entreprise

Gouvernance

Structure administrative

NUFOTEC adoptera un cadre de gestion structuré avec des professionnels qualifiés pour les rôles clés :

NUFOTEC-PHYTOMED Industries opère sous une structure de gouvernance d'entreprise basée sur les compétences et un leadership exécutif axé sur la science, conçue pour garantir la transparence, la conformité réglementaire et une croissance industrielle durable. L'entreprise est supervisée par un Conseil d'Administration professionnellement constitué qui assure une supervision stratégique, la supervision des risques et la protection des investisseurs. La direction exécutive est structurée en fonctions spécialisées couvrant les opérations, la recherche scientifique, les finances, l'assurance qualité et le développement commercial. Les activités opérationnelles sont organisées en divisions distinctes couvrant l'agriculture biologique commerciale, la transformation et la fabrication avancées, la recherche et l'innovation, la conformité réglementaire et les services corporatifs. Des mécanismes indépendants d'audit, de conformité et de supervision ESG sont intégrés au cadre de gouvernance pour garantir la responsabilité, l'intégrité institutionnelle et la résilience à long terme de l'entreprise.

Administrative Structure
No Position Qualification Major Role(s)
1 Chief Executive Officer (CEO) Overall management and decision making
2 Board of Directors Provision of strategic direction
3 Chief Operations Officer (COO) PhD in Clinical Pharmacology, Pharmacokinetics or Drug Development Overseeing production, quality control, R&D coordination, regulatory compliance, technical stuff, supply chain, facility operations, and safety
4 Finance & Administration Manager Master's degree in Business Administration or related field Management of accounting and human resources
5 Director of Quality Control Master's degree in Chemistry / Biotechnology / Food Science and Technology Overseeing of correct and efficient manufacturing-related operations
6 Director of Industrial Maintenance Master's degree in industrial maintenance, skilled in industrial automation, Good Manufacturing Practice (GMP) and Standard Operating Procedures (SOPs) Overseeing of installation, repair and maintenance of all facility's processing and research laboratory equipment
7 Head of (Research) Laboratory PhD degree in Molecular Biology / Biochemistry Overseeing lab research direction, staff supervision and lab operations compliance
8 Sales and Marketing Manager Bachelor degree in Marketing, Business Administration Management of sales team, marketing staff and distributors
9 Digital Marketing and Creative Design Manager Bachelor degree in Marketing, Communications and Graphic Design Graphic design and mass media advertising
10 Supply and Logistic Officer Bachelor degree in Logistics, Supply Chain Management Overseeing procurement control, inventory and distribution
11 Corporate Lawyer Holding Law Degree / Corporate Business Law Overseeing all company's legal matters
12 Director of Agricultural Operations Master's degree in Agricultural Engineering Overseeing the crop / medicinal plant organic industrial farming
Comités & départements

Comités de gouvernance et personnalités

Governance Committees & Personalities
Committee Responsibilities
Executive Management Committee (EMC)
  • Strategic planning & policy approval
  • Oversees departmental coordination
  • Budget & investment decisions
Governance & Compliance
  • Ensures regulatory compliance with national and international standards (e.g. ZAMRA, ZEMA, GMP, ISO)
  • Oversees ethical, legal and risk management frameworks across departments
  • Monitors internal policies and guides organizational accountabilities and transparency
Quality Management Committee (QMC)
  • Ensures GMP/ISO compliance
  • Reviews internal audits, CAPA, deviations
  • Approves changes to SOPs/QA systems
Ethics & Compliance Committee
  • Monitors regulatory, legal, and environmental compliance
  • Prevents conflicts of interest
  • Promotes ethical business conduct
Product Development / R&D Committee
  • Approves new formulations
  • Oversees clinical validation (if any)
  • Guides innovation strategy
Health & Safety Committee
  • Implements occupational health/safety policies
  • Risk assessment & emergency preparedness
  • Coordinates safety training
Departments & Responsibilities
Department Responsibilities
Production Department
  • Executes manufacturing (extraction, formulation, packaging)
  • Maintains batch records, GMP hygiene
  • Manages equipment operations
Quality Assurance (QA)
  • GMP implementation & document control (SOPs, CAPA)
  • In-process and post-production checks
  • Batch release authorization
Quality Control (QC)
  • Lab testing (raw materials, in-process, finished products)
  • Microbiology, chemical, and instrumental testing
  • Stability testing and sampling
Research & Development (R&D)
  • Product formulation & standardization
  • Pilot production and validation
  • Ingredient functionality research
Regulatory Affairs
  • Handles product registration (ZAMRA, MOH)
  • Prepares dossiers, compliance documentation
  • Communicates with relevant authorities
Supply Chain & Logistics
  • Procurement of raw materials, capsules, packaging
  • Warehouse & stock management
  • Delivery/distribution planning
Finance & Accounting
  • Manages budgeting, salaries, audits
  • Prepares financial statements
  • Handles L/Cs, T/Ts, and bank relations
Marketing and Sales
  • Develops branding & promotion strategy
  • Manages media, partnerships, and advertising
  • Supports product launch
Human Resources (HR)
  • Staff recruitment, onboarding, and training
  • Oversees compliance with labor
  • Evaluates performance & HR policies
Facility Engineering & Maintenance
  • Maintains cleanroom, HVAC, utilities
  • Ensures GMP-compliant infrastructure
  • Coordinates equipment calibration/repairs
Risk Management
  • Identifies, assesses and monitors risks that could impact operations, finance or compliance
  • Develops mitigation strategies and contingency plans to minimize potential losses
  • Ensures integration of risk controls into daily operations and strategic planning
IT & Data Systems
  • Manages data integrity, cyber security, LIMS/ERP systems
  • Supports automation and traceability
  • Digital compliance (e.g., 21 CFR Part 11)
Conformité réglementaire

Licensing and Regulatory Compliance

AGF-PHYTOMED INDUSTRIES is subjected to the following regulatory licensing:

  • Business Application & Registration – PACRA
  • Investment Licence – ZDA
  • Environmental Impact Assessment (EIA) Certificate – ZEMA
  • Screening EPB Report Certificate – ZEMA
  • Waste Management Licence – ZEMA
  • Site Approval Certificate – ZMRA
  • Product Registration – ZMRA
  • GMP Inspection – ZAMRA
  • Manufacturing Licence – ZAMRA
  • Investor Permit – Immigration
  • Product Testing & Application – ZABS
  • Factory Inspection – ZABS
  • Certification Mark – ZABS
  • Premises Hygiene Clearance Certificate – Local Health Department (Municipal/District Health Office)
  • Food Safety Inspection/Compliance Certificate – Local Health Department (Municipal/District Health Office)
  • Food Handling/Safety Certificate – Local Health Department (Municipal/District Health Office)
  • Occupational Health Risk Assessment Certificate – Local Health Department (Municipal/District)
  • Annual Health Compliance Verification – Local Health Department (Municipal/District Health Office)
  • Land Title Deeds – Headmen, Chief, District, Province & Ministry of Land
  • ISO 9001 – Quality Management System – Initial Certification
  • ISO 9001 – Quality Management System – Annual Surveillance
  • ISO 22000 – Food Safety
  • ISO 14001 – Environmental Governance and Sustainability – Initial Certification
  • ISO 14001 – Environmental Governance and Sustainability – Annual Surveillance
  • ISO 45001 – Occupational Health & Safety – Initial Certification
  • ISO 45001 – Occupational Health & Safety – Annual Surveillance Audits
  • ISO 14644 – Cleanroom Qualification ISO 5 / Room x 10
  • ISO 14644 – Cleanroom Annual Re-certification Audits ISO 5 / Room x 10
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