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1. Foreign Collaboration Clause: Required when the company plans to have foreign technical or financial collaboration

2. Research and Development Clause: Detailed section about R&D activities when the company plans significant research operations

3. Intellectual Property Rights: Specific section for companies focusing on patent development and IP-intensive activities

4. Environmental Compliance: Detailed environmental commitments for companies handling hazardous materials

5. Export-Import Activities: Required for companies planning international trade operations

6. Clinical Research: Necessary for companies planning to conduct clinical trials

1. Schedule I - Subscriber Details: Details of initial subscribers including names, addresses, occupations, and number of shares subscribed

2. Schedule II - Initial Directors: List of first directors of the company with their details and DIN numbers

3. Schedule III - Property Details: Details of any property or assets being vested in the company at formation

4. Schedule IV - Manufacturing Facilities: Details of proposed manufacturing facilities and their compliance with GMP guidelines

5. Schedule V - Product Categories: List of pharmaceutical product categories the company intends to manufacture or trade

6. Schedule VI - Technical Collaborations: Details of any technical collaborations or technology transfer agreements

7. Appendix A - Regulatory Certifications: List of required regulatory certifications and licenses to be obtained

8. Appendix B - Capital Structure: Detailed breakdown of the company's capital structure and share classes