¶¶Òõ¶ÌÊÓƵ

1. Research and Development Objects: Additional objects specifically related to pharmaceutical research and development activities, used when the company plans to conduct R&D

2. International Operations: Specific provisions for international pharmaceutical trade and operations, included when planning international business

3. Manufacturing Specifications: Detailed objects related to pharmaceutical manufacturing capabilities, included for manufacturing companies

4. Clinical Trial Provisions: Objects related to conducting clinical trials, included if the company plans to engage in clinical research

5. Intellectual Property Rights: Specific provisions regarding patent rights and intellectual property, important for companies developing new drugs

6. Environmental Compliance: Additional objects related to environmental protection and waste management, crucial for manufacturing facilities

1. Schedule 1: Initial Subscribers: Details of the initial shareholders including names, addresses, and number of shares subscribed

2. Schedule 2: Share Classes: Detailed description of different share classes, rights, and restrictions if multiple share classes exist

3. Schedule 3: Professional Qualifications: List of required professional qualifications for key positions in compliance with Pharmacists Council regulations

4. Schedule 4: Regulatory Licenses: List of required NAFDAC and other regulatory licenses and permits

5. Schedule 5: Restricted Activities: List of pharmaceutical activities requiring special permits or restricted by regulations