Update genesis/regulation.py

genesis/regulation.py

@@ -1,35 +1,61 @@
 # genesis/regulation.py
 """
-Regulatory Insights for GENESIS-AI
-Fetches approvals, clinical trial phases, and safety alerts from FDA and EMA.
+Regulatory Intelligence Module for GENESIS-AI
+Fetches or simulates biosafety, biosecurity, and biotechnology regulatory requirements
+across major jurisdictions (US, EU, WHO guidelines, etc.).
 """
 
-import requests
+import logging
 
-FDA_DRUG_API = "https://api.fda.gov/drug/drugsfda.json"
-EMA_MEDICINE_API = "https://www.ema.europa.eu/api/medicines"
+logging.basicConfig(level=logging.INFO)
 
-def fetch_fda_drug_info(drug_name):
-    """Search FDA database for a drug."""
-    try:
-        r = requests.get(FDA_DRUG_API, params={"search": f"products.brand_name:{drug_name}", "limit": 5})
-        r.raise_for_status()
-        return r.json().get("results", [])
-    except Exception as e:
-        return {"error": str(e)}
+def fetch_regulatory_info(topic: str, region: str = "global"):
+    """
+    Fetch biotechnology regulatory guidelines for a given topic.
+    This is a placeholder using static logic — can be expanded with real APIs.
+    
+    Args:
+        topic (str): The biotech topic (e.g., "CRISPR gene editing", "oncolytic viruses").
+        region (str): Region or jurisdiction (e.g., "US", "EU", "WHO", "global").
+    
+    Returns:
+        dict: Regulatory guidelines summary.
+    """
+    logging.info(f"[Regulation] Fetching regulatory info for topic '{topic}' in region '{region}'")
 
-def fetch_ema_medicine_info(medicine_name):
-    """Search EMA database for a medicine."""
-    try:
-        r = requests.get(f"{EMA_MEDICINE_API}?searchQuery={medicine_name}")
-        r.raise_for_status()
-        return r.json()
-    except Exception as e:
-        return {"error": str(e)}
+    base_guidelines = {
+        "global": [
+            "Follow WHO Laboratory Biosafety Manual (4th edition).",
+            "Adhere to Cartagena Protocol on Biosafety for GMO handling.",
+            "Implement dual-use research of concern (DURC) assessment."
+        ],
+        "US": [
+            "Comply with NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules.",
+            "Follow CDC/NIH Biosafety in Microbiological and Biomedical Laboratories (BMBL).",
+            "Check FDA regulations for clinical trials (21 CFR)."
+        ],
+        "EU": [
+            "Follow EU Directive 2009/41/EC on contained use of genetically modified micro-organisms.",
+            "Adhere to EMA clinical trial regulations.",
+            "Comply with GDPR for genetic data handling."
+        ],
+        "WHO": [
+            "Adhere to WHO guidance on responsible life sciences research.",
+            "Follow WHO pandemic preparedness frameworks."
+        ]
+    }
+
+    # Select guidelines based on region
+    guidelines = base_guidelines.get(region, base_guidelines["global"])
+
+    # Example logic for special topics
+    if "crispr" in topic.lower():
+        guidelines.append("Ensure genome editing oversight by institutional ethics boards.")
+    if "oncolytic" in topic.lower():
+        guidelines.append("Comply with additional viral vector safety assessments.")
 
-def get_regulatory_data(term):
-    """Fetch both FDA and EMA data."""
     return {
-        "fda": fetch_fda_drug_info(term),
-        "ema": fetch_ema_medicine_info(term)
+        "topic": topic,
+        "region": region,
+        "guidelines": guidelines
     }