PHARMACEUTICAL INDUSTRY

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Industry Characteristics & Challenges

Pharmaceutical manufacturing involves synthesis, fermentation, extraction, formulation, and packaging processes with stringent emission control requirements.

Solvent usage in API synthesis and coating operations generates significant VOC emissions. Powder handling creates dust control challenges.

GMP compliance and product protection add complexity to emission control system design and operation.

PHARMACEUTICAL INDUSTRY
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API Synthesis Section

Emission Characteristics

Chemical synthesis releases solvents, reaction by-products, and potentially hazardous compounds. Batch operations create variable emission profiles.

Recommended Treatment

  • Solvent recovery systems
  • Thermal oxidation (RTO/RCO)
  • Scrubber systems for specific compounds
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Formulation Section

Emission Characteristics

Tablet coating, granulation, and spray drying generate solvent vapors and fine powders. Product containment and cross-contamination prevention are priorities.

Recommended Treatment

  • Contained processing systems
  • HEPA-grade filtration
  • Solvent recovery or destruction
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Packaging Section

Emission Characteristics

Packaging operations may generate dust from powder handling and VOCs from printing and labeling. GMP requirements dictate system design.

Recommended Treatment

  • Local exhaust ventilation
  • Dust collection with product recovery
  • Clean room compatible systems

Engineering Focus for Pharmaceutical Industry

Pharmaceutical emission control must meet both environmental regulations and GMP requirements. System design priorities include containment, cleanability, and validation compliance alongside effective emission treatment.

AIER Solution Approach

AIER delivers emission control solutions designed for pharmaceutical manufacturing environments, combining regulatory compliance expertise with proven treatment technologies to protect products, workers, and the environment.