#cdsco

bisisimarkservicesbisisimarkservices
2026-02-19

CDSCO Approval & CDSCO License Guide in India 2026

From the start in 2025, clinical research organizations might qualify as CROs online through the SUGAM Portal.
For the acquisition of devices used in public health programs, new regulations calls for products that are licensed.
📞 +91 7011067811
✉️ biscro.customercare@umspcs.in

approval, approvals India, licence, registration, regulatory approval, consultant,

Read more info: umspcs.in/blog/cdsco-approval-

Mathrubhumi EnglishMathrubhumi_English
2026-02-10

AstraZeneca Pharma India has received CDSCO approval to sell and distribute Durvalumab (Imfinzi) for an additional cancer indication, expanding treatment options for endometrial cancer patients. english.mathrubhumi.com/lifest

Mathrubhumi EnglishMathrubhumi_English
2026-01-21

CDSCO flags 167 drug samples as Not of Standard Quality (NSQ) in December, including spurious drugs. Learn about the latest drug safety alerts and regulatory actions. english.mathrubhumi.com/news/i

Mathrubhumi EnglishMathrubhumi_English
2025-10-23
Mathrubhumi EnglishMathrubhumi_English
2025-10-07

AstraZeneca Pharma India receives CDSCO approval for Trastuzumab Deruxtecan for additional cancer indications english.mathrubhumi.com/news/i

2025-10-05

CDSCO Writes To Tamil Nadu FDA, Seeks Strictest Action on ‘Coldrif’ Manufacturer

CDSCO Writes To Tamil Nadu FDA, Seeks Strictest Action on ‘Coldrif’ Manufacturer --------------------------------------------------------------------------------------------------------- OdishaTV is Odisha's no 1 News Channel. OTV being the first private satellite TV channel in Odisha carries the onus of charting a course that…

odnews.in/cdsco-writes-to-tami

Mathrubhumi EnglishMathrubhumi_English
2025-10-05

The Central Drugs Standard Control Organisation (CDSCO) is set to take stringent action against Sresan Pharmaceuticals, the manufacturer of Coldrif cough syrup, following reports of several child fatalities linked to the product, ANI reported, citing sources. english.mathrubhumi.com/news/i

Royed Trainingroyedtraining
2025-06-03

🔬 Experience the real-time regulatory approval simulation and understand the significance of Form CT-07B in India's clinical trial licensing.
🎯 Decode the process.
Read now 👉 zurl.co/RtO18

Royed Trainingroyedtraining
2025-04-25

🚨 Master Regulation in India!

📘 Covers , licensing, classification, , & compliance.

✅ Perfect for RA pros & MedTech teams!

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medical device regulation in india
Royed Trainingroyedtraining
2025-03-20

Detailed insight on Form CT-07B and it's usage. Explore and download comprehensive Form CT-07B compliance checklist for CRO registration.

zurl.co/Fxi8N

Royed Trainingroyedtraining
2025-03-17

⚡Master Medical Device Regulation in India in just 1 week with Royed Training! Get hands-on expertise in CDSCO approvals, submission pathways, and compliance.
zurl.co/aOl7F

Veeda Clinical ResearchVeedacr04
2019-08-23

Roundup: India Forms Technical Advisory Group to Help

Australia’s Goods Administration (TGA) has revealed that parts of the industry objected strongly to its recently adopted standard for tablets and .

Read More: lnkd.in/er5ixzk

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