
Legislation impacting pharma manufacturing in China and India.
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£225(approx. $309)
- Posted:
- Proposals: 5
- Remote
- #4345594
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Description
Experience Level: Expert
Estimated project duration: less than 1 week
A consultant requires research on environmental legislation affecting API manufacturers in China and India. Specifically, relevant laws governing carbon emissions, wastewater treatment, solvent usage, air pollution and energy efficiency at both the national and state/provincial levels for both countries.
The researcher aims to understand how regulations impact operations for firms producing Active Pharmaceutical Ingredients. The successful candidate will identify statutes, acts and directives pertaining to each of the environmental factors (carbon emissions, wastewater, etc.) for each administrative division within China and India.
National standards will also be explored to gain insight into overarching frameworks. Finally, English translations or summaries of the key legislatives must be sourced through official government websites or databanks. The focus is on establishing a comprehensive outline of the intricate regulatory landscapes as they correspond to sustainable manufacturing practices within the pharmaceutical sector in these nations.
Topics will include analyses of pollution control boards, environmental protection agencies and other government bodies enacting statutory law. The work requires synthesizing sometimes complex legal terminology into clear and concise summaries of rules influencing this important industry across varying state and central jurisdictions.
The researcher aims to understand how regulations impact operations for firms producing Active Pharmaceutical Ingredients. The successful candidate will identify statutes, acts and directives pertaining to each of the environmental factors (carbon emissions, wastewater, etc.) for each administrative division within China and India.
National standards will also be explored to gain insight into overarching frameworks. Finally, English translations or summaries of the key legislatives must be sourced through official government websites or databanks. The focus is on establishing a comprehensive outline of the intricate regulatory landscapes as they correspond to sustainable manufacturing practices within the pharmaceutical sector in these nations.
Topics will include analyses of pollution control boards, environmental protection agencies and other government bodies enacting statutory law. The work requires synthesizing sometimes complex legal terminology into clear and concise summaries of rules influencing this important industry across varying state and central jurisdictions.
Matt P.
100% (5)Projects Completed
7
Freelancers worked with
4
Projects awarded
27%
Last project
23 Mar 2025
United Kingdom
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