Robot | Path | Permission |
GoogleBot | / | ✔ |
BingBot | / | ✔ |
BaiduSpider | / | ✔ |
YandexBot | / | ✔ |
User-agent: |
Title | KVC Consulting, |
Description | Welcome to KVC Biopharma, Welcome to KVC Biopharma, LLC Welcome to KVC Biopharma, LLC Welcome to KVC Biopharma, LLC Welcome to KVC Biopharma, LLC Early and Late Phase Drug Developm |
Keywords | N/A |
WebSite | kvcbiopharma.com |
Host IP | 13.248.243.5 |
Location | United States |
Site | Rank |
US$1,194
Last updated: 2023-05-20 04:18:00
kvcbiopharma.com has Semrush global rank of 0. kvcbiopharma.com has an estimated worth of US$ 1,194, based on its estimated Ads revenue. kvcbiopharma.com receives approximately 137 unique visitors each day. Its web server is located in United States, with IP address 13.248.243.5. According to SiteAdvisor, kvcbiopharma.com is safe to visit. |
Purchase/Sale Value | US$1,194 |
Daily Ads Revenue | US$1 |
Monthly Ads Revenue | US$33 |
Yearly Ads Revenue | US$396 |
Daily Unique Visitors | 9 |
Note: All traffic and earnings values are estimates. |
Host | Type | TTL | Data |
kvcbiopharma.com. | A | 3599 | IP: 13.248.243.5 |
kvcbiopharma.com. | A | 3599 | IP: 76.223.105.230 |
kvcbiopharma.com. | NS | 3600 | NS Record: ns36.domaincontrol.com. |
kvcbiopharma.com. | NS | 3600 | NS Record: ns35.domaincontrol.com. |
kvcbiopharma.com. | MX | 3600 | MX Record: 0 kvcbiopharma-com.mail.protection.outlook.com. |
kvcbiopharma.com. | TXT | 3600 | TXT Record: v=spf1 include:spf.protection.outlook.com -all |
kvcbiopharma.com. | TXT | 3600 | TXT Record: NETORG345863.onmicrosoft.com |
Welcome to KVC Biopharma, LLC Welcome to KVC Biopharma, LLC Welcome to KVC Biopharma, LLC Welcome to KVC Biopharma, LLC Early and Late Phase Drug Development Kathleen V. Courtemanche (919) 270-5089 BIOPHARMA SERVICES Over 30 years industry experience driving the advancement of therapeutic drugs from early pre-clinical assessment to late phase commercial licensure: -Program leadership, management, and project team support Serve as development program lead for virtual and/or growing teams Develop and manage program plans including project scope, timelines and budgets to achieve development milestones, including first in man (FIM), proof of concept (PoC), and registration enabling objectives Provide program management leadership to development functions to achieve on-time dossier submission and approval/launch (BLA/NDA/JNDA/MAA) Manage product development and manufacturing, management of studies supporting product pharmacology and safety, clinical study design and operational execution |
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